Acro-callous syndrome: A case report.
Acrocallous syndrome
Antenatal diagnosis
Embryo-fetopathy
Polymalformative syndrome
Journal
International journal of surgery case reports
ISSN: 2210-2612
Titre abrégé: Int J Surg Case Rep
Pays: Netherlands
ID NLM: 101529872
Informations de publication
Date de publication:
Jul 2022
Jul 2022
Historique:
received:
17
04
2022
revised:
30
04
2022
accepted:
14
05
2022
pubmed:
24
6
2022
medline:
24
6
2022
entrez:
23
6
2022
Statut:
ppublish
Résumé
A malformative syndrome of unknown prevalence, the diagnosis is based on morphological ultrasound and magnetic resonance imaging of the fetus. The transmission is genetic and autosomal recessive. Courtnes has established 4 diagnostic criteria to affirm the acrocal syndrome and to eliminate the amalgam with other polymalformative syndrome.
Identifiants
pubmed: 35738142
pii: S2210-2612(22)00456-4
doi: 10.1016/j.ijscr.2022.107210
pmc: PMC9218811
pii:
doi:
Types de publication
Journal Article
Langues
eng
Pagination
107210Informations de copyright
Copyright © 2022. Published by Elsevier Ltd.