Ichthyosis vulgaris (Q46635): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Ictiose vulgar é responsável por 95% de todos os casos de ictiose hereditária. É uma condição autossômica dominante devida a mutações no gene da filagrina. Ao nascimento, a pele pode parecer normal, mas torna-se gradualmente seca, áspera e escamosa, com a maioria dos sinais e sintomas aparecendo por volta dos 5 anos de idade. A ictiose vulgar pode afetar todas as partes da superfície da pele, incluindo o rosto e couro cabeludo, embora as flexuras dos membros sejam geralmente poupadas. A hiperlinearidade das palmas é uma manifestação característica. Está intimamente associada ao desenvolvimento de eczema atópico.
@@ description / en / description / en @@
+Ichthyosis vulgaris accounts for 95% of all cases of hereditary ichthyosis. It is an autosomal dominant condition due to filaggrin gene mutations. At birth the skin may appear normal but it gradually becomes dry, rough and scaly, with most signs and symptoms appearing by the age of 5. Ichthyosis vulgaris can affect all parts of the skin surface including the face and scalp though the limb flexures are usually spared. Hyperlinearity of the palms is a characteristic feature. It is closely associated with the development of atopic eczema.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/841161884
@@ Property / Canonical URI: https://id.who.int/icd/entity/841161884 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:EC20.00
@@ Property / CURIE: CID11:EC20.00 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-EC20.00
@@ Property / Canary Token: dki-india-EC20.00 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+ICD I500
@@ Property / Linked ICD 10: ICD I500 / rank @@
+Normal rank

Latest revision as of 15:21, 13 August 2026

Ichthyosis vulgaris accounts for 95% of all cases of hereditary ichthyosis. It is an autosomal dominant condition due to filaggrin gene mutations. At birth the skin may appear normal but it gradually becomes dry, rough and scaly, with most signs and symptoms appearing by the age of 5. Ichthyosis vulgaris can affect all parts of the skin surface including the face and scalp though the limb flexures are usually spared. Hyperlinearity of the palms is a characteristic feature. It is closely associated with the development of atopic eczema.

Language	Label	Description	Also known as
default for all languages	EC20.00
English	Ichthyosis vulgaris	Ichthyosis vulgaris accounts for 95% of all cases of hereditary ichthyosis. It is an autosomal dominant condition due to filaggrin gene mutations. At birth the skin may appear normal but it gradually becomes dry, rough and scaly, with most signs and symptoms appearing by the age of 5. Ichthyosis vulgaris can affect all parts of the skin surface including the face and scalp though the limb flexures are usually spared. Hyperlinearity of the palms is a characteristic feature. It is closely associated with the development of atopic eczema.