Diseases of the skin and subcutaneous tissue (dermatology)

Ectomesodermal focal dysplasia

Dysplasia ectomesodermal focal (syn: Goltz syndromes, Goltz-Gorlin syndrome, focal dermal hypoplasia, mesoectodermal dysplasia syndrome) is a rare disease, probably genetically heterogeneous, but in most cases inherited X-linked dominantly fatal in male fetuses

Children's progeria (the Hutchinson-Guildford syndrome)

Child progeria (sync Hutchinson-Guilford syndrome) is a rare, probably genetically heterogeneous disease, with a predominantly autosomal recessive type of inheritance, the possibility of a new dominant mutation is not ruled out.

Progeria of adults (Werner's syndrome)

Werner's syndrome (syn. Progeria of adults) is a rare autosomal recessive disease, the gene locus is 8p12-p11. It develops in people aged 15-20 years and is characterized by gradual progression.

Ataxia telangiectatic (Louis-Bar syndrome)

Ataxia telangiectatic (syn: Louis-Bar syndrome) is a rare systemic disease characterized by cerebellar ataxia, which is the earliest symptom, telangiectasias that appear later, usually at 4 years of age, chromosomal instability, immunodeficiency, leading to frequent infections

Perforating serpiginating elastosis: causes, symptoms, diagnosis, treatment

Elastoza perforating serpiginating (syn: keratosis follicular serpiginating Lutz, elastom intrapapillary perforating verruxiform Michera) - hereditary disease of connective tissue of unknown etiology

Elastic pseudoksantom: causes, symptoms, diagnosis, treatment

Elastic pseudoksantom (syn.: Grenblad-Strandberg syndrome, Touraine's systematized elastorexis) is a relatively rare systemic disease of the connective tissue with a predominant lesion of the skin, eyes, and cardiovascular system.

Flabby skin: causes, symptoms, diagnosis, treatment

Sluggish skin (syn: dermatochalasis, generalized elastolysis) is a heterogeneous group of generalized connective tissue diseases with general clinical and histological skin changes.

Chernogubov-Ehlers-Danlos syndrome (hyperelastic skin): causes, symptoms, diagnosis, treatment

Chernogubov-Ehlers-Danlos Syndrome (syn. Hyperelastic skin) is a heterogeneous group of hereditary connective tissue diseases characterized by a number of common clinical signs and similar morphological changes.

Bullous epidermolysis: causes, symptoms, diagnosis, treatment

Congenital bullous epidermolysis (synovial pemphigus) is a heterogeneous troupe of genetically determined diseases, among which there are both dominant and recessively inherited forms.

Pemphigus familial benign chronic: causes, symptoms, diagnosis, treatment

Pemphigus is a family benign chronic (synovial Guzhero-Hailey-Hailey disease) - an autosomal dominant inherited disease characterized by the appearance in the puberty period, but often later, of multiple flat blisters

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