| Literature DB >> 31068350 |
Farzeen Shuaib Mohtisham1,2, Adel Sallam1,2, Aiman Shawli2,3.
Abstract
Multiple pterygium syndrome of lethal type is a very rare genetic condition affecting the skin, muscles and skeleton. It is characterised by minor facial abnormalities, prenatal growth deficiency, spine defects, joint contractures, and webbing (pterygia) of the neck, elbows, back of the knees, armpits and fingers. We present a case of lethal multiple pterygium syndrome born at our hospital proven by the genetic analysis showing a double homozygous mutation. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: congenital disorders; genetic screening / counselling; musculoskeletal syndromes; neonatal intensive care
Mesh:
Substances:
Year: 2019 PMID: 31068350 PMCID: PMC6506140 DOI: 10.1136/bcr-2018-229045
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X