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Chromosomal disorder
XYYY syndrome, also known as 48,XYYY, is a chromosomal disorder in which a male has two extra copies of the Y chromosome. The syndrome is exceptionally
XYYY_syndrome
Rare chromosomal disorder
adults with XYYYY syndrome have been described. The disorder's prevalence is estimated to be below 1 in 1,000,000. XYY syndrome XYYY syndrome While some writers
XYYYY_syndrome
Genetic disorder
Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome
Down_syndrome
X chromosome monosomy
Turner syndrome (TS), commonly known as 45,X, or 45,X0, is a chromosomal disorder in which cells of females have only one X chromosome instead of two,
Turner_syndrome
Chromosomal disorder
chromosome aneuploidies, such as tetrasomy X, pentasomy X, XYYY syndrome, XYYYY syndrome, and XXXXY syndrome, are survivable with relatively mild phenotypes due
XXXYY_syndrome
Genetic condition in which a male has an extra Y chromosome
Klinefelter syndrome XXYY syndrome XYYY syndrome XXXYY syndrome XXYYY syndrome XYYYY syndrome Turner syndrome Trisomy X "47,XYY syndrome". Genetics Home
XYY_syndrome
Condition present at birth regardless of cause
as limb anomalies, syndromes involving multiple systems, and Down syndrome. Recent studies have concluded that 5–9% of Down syndrome cases are due to paternal
Birth_defect
Human chromosomal condition
with 45,X, known as Turner syndrome, XYY syndrome (known as Superman or Jacobs syndrome), 47,XXX (known as trisomy X), 48,XYYY, 48,XXYY, mosaicism 46,XY/47
XXYYY_syndrome
RV, Turner S, Ledbetter DH, Martin CL (1993). "17q12 Recurrent Deletion Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya
List_of_genetic_disorders
Sex chromosome in the XY sex-determination system
PMID 11662398. Abedi M, Salmaninejad A, Sakhinia E (January 2018). "Rare 48, XYYY syndrome: case report and review of the literature". Clinical Case Reports. 6
Y_chromosome
Natural premature termination of pregnancy
risk of miscarriage, including diabetes, endometriosis, polycystic ovary syndrome (PCOS), hypothyroidism, certain infectious diseases, and autoimmune diseases
Miscarriage
Medical condition
Fryns–Aftimos syndrome (also known as Baraitser–Winter syndrome 1, or BWS1) is a rare chromosomal condition and is associated with pachygyria, severe
Fryns–Aftimos_syndrome
Index of articles associated with the same name
Identity Development of an Adolescent Male with Emotional Disturbance and 48, XYYY Karyotype in an Institutional Setting". Qualitative Report. 17 (1): 222–243
Sex_chromosome_anomalies
Abnormal multiples of one or more chromosomes
XXXX, 48,XXXY, 48,XXYY) is more rare than 49,XXXXY. Polysomy Y (47,XYY; 48,XYYY; 48,XXYY; 49,XXYYY) occurs in 1 out of 975 males and may cause psychiatric
Polysomy
Factors that increase the chance of a miscarriage
rejection Autoimmune disorder Coeliac disease Lupus Antiphospholipid antibody syndrome Anti-thyroid autoantibodies Placenta abnormality Previous miscarriage Eating
Miscarriage_risks
Medical condition
Tetrasomy X (48,XXXX) Pentasomy X (49,XXXXX) XYY syndrome (47,XYY) XYYY syndrome (48,XYYY) XYYYY syndrome (49,XYYYY) 45,X/46,XY 46,XX/46,XY Translocations
Miscarriage and mental disorders
Miscarriage_and_mental_disorders
Presence of an abnormal number of chromosomes in a cell
found in Down syndrome, affecting 1 in 800 births. Trisomy 18 (Edwards syndrome) affects 1 in 6,000 births, and trisomy 13 (Patau syndrome) affects 1 in
Aneuploidy
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