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MAGEL2-related disorders: A study and case series.

Authors :
Patak J
Gilfert J
Byler M
Neerukonda V
Thiffault I
Cross L
Amudhavalli S
Pacio-Miguez M
Palomares-Bralo M
Garcia-Minaur S
Santos-Simarro F
Powis Z
Alcaraz W
Tang S
Jurgens J
Barry B
England E
Engle E
Hess J
Lebel RR
Source :
Clinical genetics [Clin Genet] 2019 Dec; Vol. 96 (6), pp. 493-505. Date of Electronic Publication: 2019 Aug 22.
Publication Year :
2019

Abstract

Pathogenic MAGEL2 variants result in the phenotypes of Chitayat-Hall syndrome (CHS), Schaaf-Yang syndrome (SYS) and Prader-Willi syndrome (PWS). We present five patients with mutations in MAGEL2, including the first patient reported with a missense variant, adding to the limited literature. Further, we performed a systematic review of the CHS and SYS literature, assess the overlap between CHS, SYS and PWS, and analyze genotype-phenotype correlations among them. We conclude that there is neither a clinical nor etiological difference between CHS and SYS, and propose that the two syndromes simply be referred to as MAGEL2-related disorders.<br /> (© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1399-0004
Volume :
96
Issue :
6
Database :
MEDLINE
Journal :
Clinical genetics
Publication Type :
Academic Journal
Accession number :
31397880
Full Text :
https://doi.org/10.1111/cge.13620