Cyclopia with proboscis: A rare congenital anomaly.

congenital defects cyclopia holoprosencephaly proboscis

Journal

Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 02 03 2021
revised: 31 05 2021
accepted: 01 06 2021
entrez: 23 7 2021
pubmed: 24 7 2021
medline: 24 7 2021
Statut: epublish

Résumé

Cyclopia with a proboscis, a rare congenital anomaly, and a severe form of holoprosencephaly occur as a result of incomplete separation of prosencephalon into two halves of hemispheres during organogenesis. A prenatal anomaly scan can help in the early detection of the condition and timely termination of the pregnancy.

Identifiants

pubmed: 34295488
doi: 10.1002/ccr3.4466
pii: CCR34466
pmc: PMC8283846
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e04466

Informations de copyright

© 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

None to declare.

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Clin Case Rep. 2021 Jul 16;9(7):e04466
pubmed: 34295488

Auteurs

Asma Kunwar (A)

Department of Obstetrics and Gynecology Tribhuvan University Teaching Hospital Kathmandu Nepal.

Bibek Man Shrestha (BM)

Maharajgunj Medical Campus Institute of Medicine Kathmandu Nepal.

Suraj Shrestha (S)

Maharajgunj Medical Campus Institute of Medicine Kathmandu Nepal.

Pooja Paudyal (P)

Department of Obstetrics and Gynecology Tribhuvan University Teaching Hospital Kathmandu Nepal.

Suniti Rawal (S)

Department of Obstetrics and Gynecology Tribhuvan University Teaching Hospital Kathmandu Nepal.

Classifications MeSH