Craniolenticulosutural dysplasia (Q55539): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A displasia craniolenticulosutural, também conhecida como síndrome de Boyadjiev-Jabs, é caracterizada pela associação específica de fontanelas grandes e de fechamento tardio, hipertelorismo, catarata de início precoce e displasia esquelética generalizada leve.
@@ description / en / description / en @@
+Craniolenticulosutural dysplasia, also known as Boyadjiev-Jabs syndrome, is characterised by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalised skeletal dysplasia.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/970423180
@@ Property / Canonical URI: https://id.who.int/icd/entity/970423180 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_970423180
@@ Property / CURIE: CID11:ID_970423180 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_970423180
@@ Property / Canary Token: dki-india-ID_970423180 / 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

Latest revision as of 03:11, 14 August 2026

Craniolenticulosutural dysplasia, also known as Boyadjiev-Jabs syndrome, is characterised by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalised skeletal dysplasia.

Language	Label	Description	Also known as
default for all languages	ID_970423180
English	Craniolenticulosutural dysplasia	Craniolenticulosutural dysplasia, also known as Boyadjiev-Jabs syndrome, is characterised by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalised skeletal dysplasia.