A Rare Case of Fraser Syndrome with Partial Vaginal Agenesis and Its Successful Reconstructive Cosmetic Management: A Case Report.
Cryptophthalmos
Fraser syndrome
Lotus flap
Vaginal agenesis
Journal
Journal of obstetrics and gynaecology of India
ISSN: 0971-9202
Titre abrégé: J Obstet Gynaecol India
Pays: India
ID NLM: 0374763
Informations de publication
Date de publication:
Aug 2022
Aug 2022
Historique:
received:
13
07
2020
accepted:
01
02
2021
entrez:
4
8
2022
pubmed:
5
8
2022
medline:
5
8
2022
Statut:
ppublish
Résumé
Fraser syndrome is a rare disorder with autosomal recessive inheritance having a wide spectrum of phenotypic appearances. A fourteen-year-old female presented to us with a chief complaint of acute retention of urine without any cyclical abdominal pain with syndromic appearance. She had partial vaginal agenesis which was treated by successful reconstructive surgery by lotus petal flap technique followed by recanalisation. Objective of this report is to highlight the rare disease of Fraser syndrome along with successful rare surgical management.
Identifiants
pubmed: 35923511
doi: 10.1007/s13224-021-01462-5
pii: 1462
pmc: PMC9339435
doi:
Types de publication
Case Reports
Langues
eng
Pagination
349-352Informations de copyright
© Federation of Obstetric & Gynecological Societies of India 2022.
Références
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pubmed: 25404827
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