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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

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

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

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

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

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

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

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

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

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

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

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