Craniosynostosis - anal anomalies - porokeratosis (Q94143): Difference between revisions
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Craniossinostose - anomalias anais - poroceratose, ou CDAGS, é uma condição muito rara caracterizada por craniossinostose e hipoplasia clavicular, (C), fechamento retardado da fontanela (D), anomalias anais (A), malformações geniturinárias (G) e erupção cutânea (S). | |||
| description / en | description / en | ||
Craniosynostosis - anal anomalies - porokeratosis, or CDAGS, is a very rare condition characterised by craniosynostosis and clavicular hypoplasia, (C), delayed closure of the fontanel (D), anal anomalies (A), genitourinary malformations (G) and skin eruption (S). | |||
Revision as of 09:15, 16 August 2026
Craniosynostosis - anal anomalies - porokeratosis, or CDAGS, is a very rare condition characterised by craniosynostosis and clavicular hypoplasia, (C), delayed closure of the fontanel (D), anal anomalies (A), genitourinary malformations (G) and skin eruption (S).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2106621307 |
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| English | Craniosynostosis - anal anomalies - porokeratosis |
Craniosynostosis - anal anomalies - porokeratosis, or CDAGS, is a very rare condition characterised by craniosynostosis and clavicular hypoplasia, (C), delayed closure of the fontanel (D), anal anomalies (A), genitourinary malformations (G) and skin eruption (S). |
