Hand and foot malformations
Gene: GSCEnsemblGeneIds (GRCh38): ENSG00000133937
EnsemblGeneIds (GRCh37): ENSG00000133937
OMIM: 138890, Gene2Phenotype
GSC is in 6 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities (SAMS) is an autosomal recessive multiple congenital anomaly syndrome with features of a first and second branchial arch syndrome. Craniofacial abnormalities can lead to conductive hearing loss, respiratory insufficiency, and feeding difficulties. Additional features include rhizomelic skeletal anomalies as well as abnormalities of the shoulder and pelvic joints. Affected individuals may also have some features of a neurocristopathy or abnormal mesoderm development, such as urogenital anomalies, that are distinct from other branchial arch syndromes.
Three unrelated families reported in 2013.Created: 31 Jul 2021, 6:14 a.m. | Last Modified: 31 Jul 2021, 6:14 a.m.
Panel Version: 0.8580
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities, MIM# 602471
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert list
- Expert Review Green
- Expert Review Green
- Victorian Clinical Genetics Services
- Phenotypes
-
- Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities, MIM# 602471
- OMIM
- 138890
- Clinvar variants
- Variants in GSC
- Penetrance
- None
- Panels with this gene
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: GSC was added gene: GSC was added to Hand and foot malformation. Sources: Expert Review Green,Expert list Mode of inheritance for gene: GSC was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: GSC were set to Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities, MIM# 602471