Phocomelia, Schinzel type (Q94205): Difference between revisions

← Older edit

@@ Property / Canary Token @@
+dki-india-ID_1732271544
@@ Property / Canary Token: dki-india-ID_1732271544 / 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 +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++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

Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterised by skeletal malformations including intercalary limb deficiencies (phocomelia sometimes combined with polydactyly, oligodactyly or ectrodactyly), absent or hypoplastic pelvic bones (including sacral agenesis or hypoplasia), skull defects (frequently a defect of the occipital bone with or without meningocele).

Language	Label	Description	Also known as
default for all languages	ID_1732271544
English	Phocomelia, Schinzel type	Schinzel phocomelia syndrome, also called limb/pelvis hypoplasia/aplasia syndrome, is characterised by skeletal malformations including intercalary limb deficiencies (phocomelia sometimes combined with polydactyly, oligodactyly or ectrodactyly), absent or hypoplastic pelvic bones (including sacral agenesis or hypoplasia), skull defects (frequently a defect of the occipital bone with or without meningocele).