Shprintzen-Goldberg omphalocele syndrome (Q94217): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Síndrome de onfalocele de Shprintzen-Goldberg é uma síndrome de malformação hereditária muito rara caracterizada por onfalocele, escoliose, características dismórficas leves (fissuras palpebrais inclinadas para baixo, pálpebras em forma de S e lábio superior fino), hipoplasia laríngea e faríngea e dificuldades de aprendizagem.
@@ description / en / description / en @@
+Shprintzen  Goldberg omphalocele syndrome is a very rare inherited malformation syndrome characterised by omphalocele, scoliosis, mild dysmorphic features (downslanted palpebral fissures, s-shaped eyelids and thin upper lip), laryngeal and pharyngeal hypoplasia and learning disabilities.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1570235082
@@ Property / Canonical URI: https://id.who.int/icd/entity/1570235082 / rank @@
+Normal rank
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+CID11:ID_1570235082
@@ Property / CURIE: CID11:ID_1570235082 / rank @@
+Normal rank
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+dki-india-ID_1570235082
@@ Property / Canary Token: dki-india-ID_1570235082 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
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@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
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++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 09:20, 16 August 2026

Shprintzen Goldberg omphalocele syndrome is a very rare inherited malformation syndrome characterised by omphalocele, scoliosis, mild dysmorphic features (downslanted palpebral fissures, s-shaped eyelids and thin upper lip), laryngeal and pharyngeal hypoplasia and learning disabilities.

Language	Label	Description	Also known as
default for all languages	ID_1570235082
English	Shprintzen-Goldberg omphalocele syndrome	Shprintzen Goldberg omphalocele syndrome is a very rare inherited malformation syndrome characterised by omphalocele, scoliosis, mild dysmorphic features (downslanted palpebral fissures, s-shaped eyelids and thin upper lip), laryngeal and pharyngeal hypoplasia and learning disabilities.