Laurin-Sandrow syndrome (Q84233): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome de Laurin-Sandrow é uma síndrome de anomalias do desenvolvimento caracterizada por polissindactilia completa das mãos, pés em espelho e anomalias do nariz (hipoplasia da asa do nariz e columela curta), frequentemente associada a duplicação ulnar e/ou fibular (e às vezes agenesia tibial).
@@ description / en / description / en @@
+Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis).
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/671594481
@@ Property / Canonical URI: https://id.who.int/icd/entity/671594481 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_671594481
@@ Property / CURIE: CID11:ID_671594481 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_671594481
@@ Property / Canary Token: dki-india-ID_671594481 / 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 09:35, 15 August 2026

Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis).

Language	Label	Description	Also known as
default for all languages	ID_671594481
English	Laurin-Sandrow syndrome	Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis).