Reference for GENODERMATOSIS. Search for GENODERMATOSIS

AI searches containing GENODERMATOSIS

GENODERMATOSIS

Genodermatosis

Genetic skin disease

different types of genodermatosis; the prevalence of genodermatosis ranges from 1 per 6000 people to 1 per 500,000 people. Genodermatosis has influence on

Genodermatosis

Bull Terrier

Dog breed

acrodermatitis, also known as Acrodermatitis of the Bull Terrier is a rare genodermatosis monogenic autosomal inherited disease found exclusively in white Bull

Bull Terrier

Bull_Terrier

Naked foal syndrome

Genetic disorder in Akhal-Teke horses

is a genetic disorder specific to the Akhal-Teke horse breed. A rare genodermatosis, it is characterized by almost complete hairlessness and mild ichthyosis

Naked foal syndrome

Naked_foal_syndrome

Miniature Bull Terrier

Dog breed

acrodermatitis, also known as Acrodermatitis of the Bull Terrier is a rare genodermatosis monogenic autosomal inherited disease found exclusively in white Bull

Miniature Bull Terrier

Miniature_Bull_Terrier

Keratolytic winter erythema

Genetic disorder causing redness and peeling of the skin on the palms and soles

prominence and severity usually occurs during winter. It is a type of genodermatosis. The name "Oudtshoorn skin" derives from the town of Oudtshoorn in the

Keratolytic winter erythema

Keratolytic_winter_erythema

Palmoplantar keratoderma

Abnormal thickening of skin in the palms or soles

previously known: frequently degenerative sclero-atrophying and keratodermic genodermatosis of the extremities]". La Semaine des Hopitaux (in French). 44 (8): 481–8

Palmoplantar keratoderma

Palmoplantar_keratoderma

Helene Ollendorff Curth

American dermatologist (1899–1982)

Abraham Buschke Academic work Discipline Dermatology Sub-discipline Genodermatosis Institutions Rudolf-Virchow-Krankenhaus, Berlin Columbia University

Helene Ollendorff Curth

Helene_Ollendorff_Curth

Inherited disorders of trafficking

and Keratoderma Syndrome) is a rare inherited genetic skin condition (Genodermatosis) which has been associated with a loss-of-function mutation in SNAP29;

Inherited disorders of trafficking

Inherited_disorders_of_trafficking

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome

Medical condition

transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis". Am. J. Hum. Genet. 86 (4): 596–603. doi:10.1016/j.ajhg.2010.02.018

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome

Keratosis_linearis_with_ichthyosis_congenita_and_sclerosing_keratoderma_syndrome

Dyschromatosis universalis hereditaria

Medical condition

with mutations in genes SASH1 and ABCB6.[citation needed] It is a rare genodermatosis. James, William D.; Elston, Dirk; Treat, James R.; Rosenbach, Misha

Dyschromatosis universalis hereditaria

Dyschromatosis_universalis_hereditaria

Haber syndrome

Medical condition

characterized by reticulated pigmentation of the person's skin. A rare genodermatosis, its key features include "rosacea-like facial eruption[,] reticulated

Haber syndrome

Haber_syndrome

White sponge nevus

Benign lesions on the insides of the cheeks

It could be classified as a skin condition, or more precisely as a genodermatosis (a genetically determined skin disorder). There are no specific treatments

White sponge nevus

White_sponge_nevus

Kindler syndrome

Medical condition

types with only 400 cases known worldwide. It is an autosomal recessive genodermatosis. The KIND1 gene mutated in Kindler syndrome codes for the protein kindlin-1

Kindler syndrome

Kindler_syndrome

Progeroid syndromes

Range of genetic disorders which cause a person to appear to grow older faster

contracture syndrome, is a rare, lethal autosomal recessive perinatal genodermatosis. Two known causes of RD are mutations in the LMNA gene, which lead to

Progeroid syndromes

Progeroid_syndromes

TGM5

mutations can cause acral peeling skin syndrome, an autosomal recessive genodermatosis characterized by the shedding of the outer epidermis. In the acral form

TGM5

Folliculin

Protein-coding gene

Matrosova V, Toro JR, et al. (October 2001). "Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps

Folliculin

Gerodermia osteodysplastica

Medical condition

Congenital malformations and deformations of integument / skin disease Genodermatosis Congenital ichthyosis/ erythrokeratodermia AD Ichthyosis vulgaris AR

Gerodermia osteodysplastica

Gerodermia_osteodysplastica

Trichorrhexis invaginata

Medical condition

proximal portion of the shaft. "Bamboo hair" is a rare autosomal recessive genodermatosis characterized by congenital ichthyosiform erythroderma, trichorrhexis

Trichorrhexis invaginata

Trichorrhexis_invaginata

Acrokeratoelastoidosis of Costa

Medical condition

instances of irregular cases, acrokeratoelastoidosis is thought to be a genodermatosis with autosomal dominant inheritance, though anecdotal reports of an

Acrokeratoelastoidosis of Costa

Acrokeratoelastoidosis_of_Costa