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Delayed development in children
Global developmental delay is an umbrella term used when children are significantly delayed in two or more areas of development. It can be diagnosed when
Global_developmental_delay
Topics referred to by the same term
The term developmental delay can refer to: Global developmental delay, an umbrella term used when children are significantly delayed in two or more areas
Developmental_delay
Disability beginning before adulthood
child's development is sometimes referred to as global developmental delay. The most common developmental disabilities are: Motor disorders, and learning difficulties
Developmental_disability
Child is late reaching development stages
A delayed milestone, which is also known as a developmental delay, refers to a situation where a child does not reach a particular developmental milestone
Delayed_milestone
Loss of developmental skills in children
It differs from global developmental delay in that a child experiencing developmental delay is either not reaching developmental milestones or not progressing
Developmental_regression
Neurodevelopmental disorder chiefly affecting motor skills
Developmental coordination disorder (DCD), also known as developmental motor coordination disorder, developmental dyspraxia, or simply dyspraxia (from
Developmental coordination disorder
Developmental_coordination_disorder
Language disorder marked by delayed language development
language delay is a language disorder in which a child fails to develop language abilities at the usual age-appropriate period in their developmental timetable
Language_delay
Human genetic disorder
MAGEL2. Main signs of this disorder are: intellectual disability/developmental delay, autism spectrum disorder, hypogonadism, hypotonia in infancy with
Schaaf–Yang_syndrome
Congenital extreme form of developmental delay and neoteny
a possibly genetic syndrome that presents as an extreme form of developmental delay, with the defining characteristic being neoteny of the patient. It
Neotenic_complex_syndrome
Medical condition
Wiedemann–Steiner syndrome (WSS) is a rare genetic disorder that causes developmental delay, unusual facial features, short stature, and reduction in muscle
Wiedemann–Steiner_syndrome
Rare condition caused by a microdeletion on the short arm of chromosome 16
arm of chromosome 16. Most affected individuals experience global developmental delay and intellectual disability, as well as childhood-onset obesity.
16p11.2_deletion_syndrome
Medical condition
SLC6A8. The main symptoms of CTD are intellectual disability and developmental delay, and these are caused by a lack of creatine in the brain, due to
Cerebral_creatine_deficiency
Medical condition
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) is a very rare genetic disorder. This disorder is one that affects bone
Severe achondroplasia with developmental delay and acanthosis nigricans
Severe_achondroplasia_with_developmental_delay_and_acanthosis_nigricans
State of low muscle tone
timeframe after birth. Most low-tone infants have delayed developmental milestones, but the length of delay can vary widely. Motor skills are particularly
Hypotonia
Neurodegenerative disorder with brain iron accumulation
neurodegeneration. Patients with BPAN develop symptoms, such as early-onset developmental delay, seizures, and further neurological decline, such as dystonia, parkinsonism
Beta-propeller protein-associated neurodegeneration
Beta-propeller_protein-associated_neurodegeneration
Language development delay, usually observed in children
child that has a speech delay due to physical malformations and children that have also been diagnosed with a developmental delay such as autism or a language
Speech_delay
Medical condition
a rare multi-systemic genetic disorder which is characterized by developmental delay, seizures, hypotonia and heart, urinary, and gastrointestinal abnormalities
Multiple congenital anomalies-hypotonia-seizures syndrome
Multiple_congenital_anomalies-hypotonia-seizures_syndrome
Rare genetic condition involving intestinal atresia, eye abnormalities and microcephaly
the eye is typically underdeveloped, and there is usually moderate developmental delay. Less common features include an atrial septal defect, increased
Strømme_syndrome
Form of child abuse
The developmental delay may be caused by a genetic disorder, disease or physical, sexual or emotional abuse. Of course, the developmental delay may be
Child_neglect
Retention of juvenile traits into adulthood
attitudes and behaviors into later adulthood" — is actually a valuable developmental characteristic, which he calls psychological neoteny. The ability of
Neoteny_in_humans
Stages in the development of children
coincidental. The developmental delay may be caused by a genetic disorder, disease or physical, sexual or emotional abuse. The developmental delay may be caused
Child_development
Presence of abundant hair between the eyebrows
105 (with hypopituitarism) Developmental delay with variable intellectual disability and dysmorphic facies Developmental delay, impaired speech, and behavioral
Unibrow
Medical condition
Pancytopenia is a medical condition in which there is significant reduction in the number of almost all blood cells (red blood cells, white blood cells
Pancytopenia
Medical condition
Specific developmental disorders (SDD) was a classification of disorders characterized by delayed development in one specific area or areas. Specific developmental
Specific developmental disorder
Specific_developmental_disorder
Rare neurodevelopmental disorder
can range from mild to severe global developmental delay and intellectual disability, usually including speech delay and impairment. Patients with JS may
Jordan's_syndrome
Rapid physical, psychological and social growth
after birth. Developmental delay is divided into Global Developmental Delay (GDD) and Intellectual Disability (ID). Global Developmental Delay is defined
Early_childhood_development
Medical condition
have normal intellect or have cognitive impairments, may experience developmental delay, or may have severe behavioral problems. Many individuals have hearing
Mucopolysaccharidosis
Medical condition
chromosome 13. The condition is primarily characterized by global developmental delay, varying degrees of intellectual disability, and severe speech and
CHAMP1-related neurodevelopmental disorder
CHAMP1-related_neurodevelopmental_disorder
Medical condition
characterised by developmental delay, intellectual disability and decreased visual acuity. All patients described have suffered from developmental delay, intellectual
Bosch–Boonstra–Schaaf optic atrophy syndrome
Bosch–Boonstra–Schaaf_optic_atrophy_syndrome
Medical condition
associated with a variable phenotype including one or more of speech delay, developmental delay, mild dysmorphism, with prominent forehead and arched eyebrows
8p23.1_duplication_syndrome
Lingering symptoms of controlling belief systems
cognitive, affective, functional, and social/cultural issues as well as developmental delays. RTS occurs in response to two-fold trauma: first the prolonged abuse
Religious_trauma_syndrome
Genetic condition involving hearing loss and depigmentation
that can result in central nervous system (CNS) symptoms such as developmental delay and muscle tone abnormalities. The syndrome is caused by mutations
Waardenburg_syndrome
Skull malformation such that one side is flattened
Craniosynostosis (nonsyndromic) 6 Developmental and epileptic encephalopathy, 1, 65, 77, and 84 Developmental delay with variable intellectual impairment
Plagiocephaly
Generalized neurodevelopmental disorder
or adolescence (onset during developmental phase). DSM-5-TR also makes a separate diagnosis of global developmental delay, reserved for children younger
Intellectual_disability
Rare genetic disorder
variants of the KMT2E gene. The clinical features generally include developmental delay, intellectual disability, decreased muscle tone, sleep disturbances
O'Donnell-Luria–Rodan syndrome
O'Donnell-Luria–Rodan_syndrome
Genetic condition causing non-cancerous tumours
skin. Symptoms may include seizures, intellectual disability, and developmental delay. TSC has autosomal dominant inheritance, meaning a child with TSC
Tuberous_sclerosis
Neurodevelopmental disorder
microcephaly, short stature, and developmental delay. Patients develop seizures that may be hard to control. Brain imaging shows delayed myelination and hypomyelination
5,10-methenyltetrahydrofolate synthetase deficiency
5,10-methenyltetrahydrofolate_synthetase_deficiency
United States law
of IDEA also allows states to define "developmental delay" (either as a standard deviation or a percent delay in chronological months) for eligibility
Individuals with Disabilities Education Act
Individuals_with_Disabilities_Education_Act
X-linked recessive disorder characterised by developmental delay
a rare X-linked genetic disorder that is mostly characterized as developmental delay. It is one of the rare causes of short stature. It is closely related
Say–Meyer_syndrome
Rare neurodevelopmental disorder
neurodevelopmental syndrome, is an ultra-rare genetic disorder characterized by developmental delay and variable intellectual disability, particularly affecting speech
Chopra–Amiel–Gordon_syndrome
Rare disease
monogenetic developmental and epileptic encephalopathy that affects the central nervous system. The broad phenotype includes global developmental delay, intellectual
TRPM3-related neurodevelopmental disorder
TRPM3-related_neurodevelopmental_disorder
Medical condition
neurodevelopmental and physical symptoms, including cognitive impairments, developmental delays, autism spectrum disorder (ASD), attention deficit hyperactivity
Fetal valproate spectrum disorder
Fetal_valproate_spectrum_disorder
Former institution for intellectually disabled children
intellectually limited as the term "developmental delay" would indicate. Some had cerebral palsy, a developmental disability that can be accompanied by
Willowbrook_State_School
Medical condition
been reported by 2018. Clinical features include Global developmental delay Significant speech delay Hypotonia Micrognathia Scoliosis Defects in motor function
Lamb–Shaffer_syndrome
Rare genetic syndrome
(tables 1 and 2). Patients are consistently characterized by global developmental delay, intellectual disability, speech abnormalities, ASD-like behaviors
22q13_deletion_syndrome
Highly focused interests most common in autistic people
Pilot Study Using the Special Interests Survey". Journal of Autism and Developmental Disorders. 51 (8). Springer Nature: 2711–2724. doi:10.1007/s10803-020-04743-6
Special_interest_(autism)
Institution for developmentally delayed people in Jacksonville, Illinois, U.S.
The Jacksonville Developmental Center was an institution for developmentally delayed clients, located in Jacksonville, Illinois. It was open from 1851
Jacksonville Developmental Center
Jacksonville_Developmental_Center
Medical condition
including adults) with this disorder usually show: Widespread developmental delay Speech delay Balance and walking difficulties (may learn to walk at a later-than-average
PURA_syndrome
Any disorder affecting the ability to comprehend or use language and speech
pathology – an abnormality of the cartilage on the vocal folds. Developmental delay – when a child fails to develop (whether that be mentally or physically)
Communication_disorder
Legal document for special education
hearing impairments, deafness, visual impairment, deaf-blindness, developmental delay, speech/language impairment, or traumatic brain injury. The IEP describes
Individualized Education Program
Individualized_Education_Program
Neurological disease
communication skills, difficulty standing or walking, as well as developmental delay. SLC13A5 Epilepsy is due to dysfunction of the SLC13A5 gene, typically
SLC13A5 citrate transporter disorder
SLC13A5_citrate_transporter_disorder
Medical condition
express the following symptoms with varying levels of severity: developmental delay and regression, intellectual disability, and abnormalities in expressive
Creatine_transporter_defect
Medical condition
result in dysmorphisms in the skull, nervous system problems, and developmental delay. Dysmorphisms in the heart, kidneys, and musculoskeletal system may
Trisomy_9
Medical condition
CdLS include thick or long eyebrows, a small nose, small stature, developmental delay, long or smooth philtrum, thin upper lip and downturned mouth. The
Cornelia_de_Lange_syndrome
Rare genetic developmental disease
WOREE syndrome, is a rare genetic developmental disorder. Its effects include drug-resistant epilepsy, developmental delay, ataxia, and premature death at
WOREE_syndrome
Medical condition
Pitt–Hopkins syndrome (PTHS) is a rare genetic disorder characterized by developmental delay, moderate to severe intellectual disability, distinctive facial features
Pitt–Hopkins_syndrome
Disability therapy profession
variety of causes, such as a stroke, brain injury, hearing loss, developmental delay, a cleft palate, cerebral palsy, or emotional issues. A common misconception
Speech–language_pathology
Medical condition
disease, feeding difficulties, cryptorchidism, joint hypermobility, developmental delay, hypotonia, and behavioral difficulties. Other common symptoms are
Kabuki_syndrome
Genetic disorder
different systems of the human body. It is mainly characterized by developmental delay, intellectual disability, craniofacial abnormalities and commonly
White–Sutton_syndrome
Rare genetic disorder
presentation varies among individuals, but typically includes global developmental delay, slow progress in mental and physical activities, syndromic autism
Beck–Fahrner_syndrome
Involuntary urination while asleep
Complications can include urinary tract infections. Most bedwetting is a developmental delay—not an emotional problem or physical illness. Only a small percentage
Nocturnal_enuresis
Scientific study of psychological changes in humans over the course of their lives
Developmental psychology is the scientific study of how and why the human mind grows, changes, and adapts over the course of a human lifetime. Originally
Developmental_psychology
Medical condition
in one or both eyes, as a result of optic nerve underdevelopment. Developmental delays are more common in children with bilateral optic nerve hypoplasia
Septo-optic_dysplasia
Medical condition
mutations will be manifested by neurodevelopmental phenotype including developmental delay, intellectual disability, hypotonia, and seizures, among other characteristics
HNRNPH2-related_disorders
Underdevelopment of the optic nerve
is often associated with endocrinopathies (hormone deficiencies), developmental delay, and brain malformations. The optic nerve, responsible for transmitting
Optic_nerve_hypoplasia
Medical condition
present with excessive orotic acid in the urine, failure to thrive, developmental delay, and megaloblastic anemia which cannot be cured by administration
Orotic_aciduria
X-linked dominant genetic disorder
problems and vomiting, but all developmental delays are subtle. By a year, language delays begin to be noticeable. These delays are followed by an increased
Fragile_X_syndrome
Autosomal recessive metabolic disorder
Patients with intermediate MSUD may be presented with acidosis and developmental delay. Contrary to classic and intermediate MSUD, intermittent MSUD individuals
Maple_syrup_urine_disease
Genetic disorder
initial diagnosis of WS. Developmental delays are present in most cases of WS, and include delay of language abilities and delayed motor-skill development
Williams_syndrome
Sister of John F. Kennedy (1918–2005)
senators Robert F. and Ted Kennedy. As a child she reportedly exhibited developmental delays. In her young adult years, she became "increasingly irritable and
Rosemary_Kennedy
Human vocal communication using spoken language
disorders can also result from stroke, brain injury, hearing loss, developmental delay, a cleft palate, cerebral palsy, or emotional issues. Speech-related
Speech
Abnormally strong sensation of hunger or desire to eat
adiposa congenita Intellectual developmental disorder, autosomal dominant 1 Obesity, hyperphagia, and developmental delay (OBHD) Rapid-onset obesity with
Polyphagia
Medical condition
rare chromosomal abnormality is often diagnosed after birth when developmental delay, irregular facial features, structural irregularities within the
Monosomy_9p
Genetic condition, the most common form of dwarfism
including hypochondroplasia and SADDAN (severe achondroplasia with developmental delay and acanthosis nigricans), a rare disorder of bone growth characterized
Achondroplasia
Support and educational system for very young children
children who have developmental delays or disabilities. Some states and regions have chosen to focus these services on children with developmental disabilities
Early_childhood_intervention
Metabolic disorders in which porphyrins build up in the body
Hepatic Autosomal dominant Photosensitivity, neurologic symptoms, developmental delay 1 in 300 in South Africa 1 in 75,000 in Finland Erythropoietic protoporphyria
Porphyria
Medical condition
children get older, they start showing developmental delay and neurobehavioral difficulties. Gross motor delay is very common; for instance independent
DeSanto–Shinawi_syndrome
Psychological disorder that can affect children
communicative efforts. It is differentiated from pervasive developmental disorder or developmental delay and from possibly comorbid conditions such as intellectual
Reactive_attachment_disorder
Rare genetic disorder
Clinically, patients present with microcephaly and significant developmental delay. While some patients may be able to walk, others may not due to spasticity
SPATCCM
Developmental disorder; related to autism
pervasive developmental disorders (PDD), as opposed to specific developmental disorders (SDD), was a group of disorders characterized by delays in the development
Pervasive developmental disorder
Pervasive_developmental_disorder
Rare metabolic genetic disorder resulting in leukoencephalopathy
spasticity, psychomotor retardation, leukoencephalopathy and global developmental delay. RPI can be diagnosed by gene sequencing or increased polyol levels
Ribose-5-phosphate isomerase deficiency
Ribose-5-phosphate_isomerase_deficiency
Genetic disorder that primarily affects the eye
Norrie disease can also have cognitive and behavioral symptoms. Developmental delay or learning difficulties are present in about 30 to 50% of males
Norrie_disease
Rare genetic disorder
pathogenic variants of the WDR26 gene. It is characterized by global developmental delay, intellectual disability, friendly demeanor, unusual walking, seizures
Skraban–Deardorff_syndrome
Irish actor (born 1976)
syndrome, a rare genetic disorder characterised by intellectual and developmental delay, lack of speech, and an excitable demeanour. From 2007 to 2008, Farrell
Colin_Farrell
Medical condition
producing an aged appearance, growth failure, hypotonia, global developmental delays, cryptorchidism, and spontaneous cardiac arrhythmias. The first family
Ogden_syndrome
Condition involving social and behavioral differences
"Practitioner Review: Self-injurious behaviour in children with developmental delay". Journal of Child Psychology and Psychiatry (Review). 56 (10): 1042–54
Autism
Excessive information sharing
outdated topics Delayed gratification Auditory processing disorder Deficits in attention, motor control and perception Developmental coordination disorder
Infodumping
Species of beetle (southern masked chafer)
in the soil called milky spore (Paenibacillus popilliae) causes a developmental delay in the larvae, and it was these infected larvae that the researchers
Cyclocephala_lurida
Medical condition
autosomal recessive progressive neurological disorder characterized by developmental delay, severe intellectual disability, seizures, and skin pigmentation
Salt_and_pepper_syndrome
Genetic disorder
syndrome, is a rare neurodevelopmental disorder characterized by developmental delay/intellectual disability, facial dysmorphisms, and short stature.
Witteveen–Kolk_syndrome
Medical condition
symptoms, but all patients generally have mild chondrodysplasia, developmental delays, and mild dysmorphic facial features such as prominent nose. As of
Ververi–Brady_syndrome
Genetic disorder caused by a mutation of chromosome 15
the UBE3A gene. 100% of AS diagnoses have the following symptoms: developmental delay: considered to be functionally severe; includes the inability for
Angelman_syndrome
Medical condition
disorders or language delays. Communication disorders or developmental language delays may occur for several different reasons. Language delays may be associated
Muteness
Group of conditions resulting from maternal alcohol consumption during pregnancy
or impulsivity Developmental language disorder Hearing loss Visual impairment, including blindness or astigmatism Developmental delay, cognitive disorder
Fetal alcohol spectrum disorder
Fetal_alcohol_spectrum_disorder
Medical condition caused by receiving too little or too many nutrients
Israa; Liu, Qin; Long, Qian; Nabwera, Helen (October 12, 2023). Cochrane Developmental, Psychosocial and Learning Problems Group (ed.). "The impact of growth
Malnutrition
Genetic disorder
characterized by hypotonia, global developmental delay, severely impaired intellectual development with poor or absent speech, delayed walking or inability to walk
RNU4-2_syndrome
Genetic disorders
CACNA1C-related disorders are primarily neurological and may include developmental delay, autism or autistic features, and seizures. Facial dysmorphism may
CACNA1C-related_disorders
Neural tube defect in which the brain protrudes out of the skull
abnormally small head), ataxia (uncoordinated muscle movement), developmental delay, vision problems, mental and growth retardation, and seizures.[citation
Encephalocele
could possibly be displaying signs of global developmental delay. Having language-related developmental delays in childhood could cause problems in a child's
Developmental_linguistics
Clinical observation of autistic traits
and not be better explained by intellectual disability or global developmental delay. Several factors make autism spectrum disorder (ASD) difficult to
Diagnosis_of_autism
DEVELOPMENTAL DELAY
DEVELOPMENTAL DELAY
Girl/Female
Assamese, Bengali, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Oriya, Sanskrit, Sindhi, Tamil, Telugu
Progress; Development; Improvement
Girl/Female
Indian
Altitude, Height, High, Development
Girl/Female
Muslim
Altitude, Height, High, Development
Boy/Male
Hindu
Development, Expanding
Boy/Male
Hindu
Development or expanding
Boy/Male
Indian, Sanskrit
Development; Expansion
Girl/Female
Hindu, Indian
Development
Girl/Female
Hindu, Indian
Development; Improvement; Progress
Boy/Male
Hindu
Development, Prosper
Boy/Male
Tamil
Development, Expanding
Boy/Male
Hindu, Indian
Development
Boy/Male
Hindu
Development, Prosper
Boy/Male
Tamil
Development or expanding
Boy/Male
Bengali, Indian
Development of God
Boy/Male
Indian
Altitude, Height, High, Development
Boy/Male
Arabic, Muslim, Sindhi
Dignity; Development
Boy/Male
Tamil
Development, Prosper
Boy/Male
Bengali, Indian
Development; Brightness
Boy/Male
Muslim
Altitude, Height, High, Development
Boy/Male
Tamil
Development, Prosper
DEVELOPMENTAL DELAY
DEVELOPMENTAL DELAY
Boy/Male
Hindu
Devoted to truth
Boy/Male
Gaelic Scottish Greek
A Scottish Gaelicfrom the Greek meaning defender of man.
Boy/Male
Arabic, Hindu, Indian, Muslim
Light
Boy/Male
Arabic, Gujarati, Hindu, Indian, Malaysian
Pretty
Boy/Male
Indian, Punjabi, Sanskrit, Sikh
Knowledge; Intelligent; Understanding
Girl/Female
Gujarati, Hindu, Indian
Waiting
Girl/Female
Muslim
Island
Girl/Female
Muslim
Love, Thirsty
Boy/Male
Hindu, Indian, Malayalam, Sanskrit
Courageous; Name of God Hanuman; No Fear
Boy/Male
Muslim
Gift of God
DEVELOPMENTAL DELAY
DEVELOPMENTAL DELAY
DEVELOPMENTAL DELAY
DEVELOPMENTAL DELAY
DEVELOPMENTAL DELAY
n.
A growth or development inward.
n.
The act of developing or disclosing that which is unknown; a gradual unfolding process by which anything is developed, as a plan or method, or an image upon a photographic plate; gradual advancement or growth through a series of progressive changes; also, the result of developing, or a developed state.
n.
The elaboration of a theme or subject; the unfolding of a musical idea; the evolution of a whole piece or movement from a leading theme or motive.
n.
The development of the spermatozoids.
n.
Life development generally.
n.
Development; disclosure; discovery.
n.
Development of cells in animal and vegetable organisms. See Gemmation, Budding, Karyokinesis; also Cell development, under Cell.
n.
Plot; action; construction; manner of development.
n.
The development of cartilage.
n.
That which promotes development or growth.
n.
The series of changes which animal and vegetable organisms undergo in their passage from the embryonic state to maturity, from a lower to a higher state of organization.
n.
Failure or lack of development.
n.
The equivalent expression into which another has been developed.
n .
Cell production or development; cytogenesis.
n.
The origin and development of blood.
a.
Pertaining to, or characteristic of, the process of development; as, the developmental power of a germ.
a.
Having two modes of embryonic development.
n.
The act or process of changing or expanding an expression into another of equivalent value or meaning.
n.
Growth or development of new material; neoplasty.
n.
Indistinctness; want of development.