Variants of the GNAI1 gene manifest as Prader-Willi-like syndrome: Case report with literature review
Clin Dysmorphol
.
2024 Apr 1;33(2):69-74.
doi: 10.1097/MCD.0000000000000491.
Epub 2024 Feb 28.
Authors
Fatima AbdulAziz AlAli
1
,
Taqwa Drdir
2
,
Amna Yahya
2
,
Elham Al Amiri
3
Affiliations
1
Pediatric Clinical Genetic Unit.
2
Pediatric Department.
3
Pediatric Endocrinology Unit, Al Qassimi Women and Children Hospital, EHS, Sharjah, United Arab Emirates.
PMID:
38441201
DOI:
10.1097/MCD.0000000000000491
No abstract available
Publication types
Review
Case Reports
MeSH terms
Chromosome Disorders*
Developmental Disabilities*
Facies*
Humans
Hypopituitarism*
Imprinting Disorders*
Syndrome*
Substances
Schaaf-Yang syndrome