Sign Up to like & get
recommendations!
0
Published in 2022 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.1932
Abstract: Schaaf‐Yang syndrome (SYS) is a rare hereditary disease caused by truncating point mutations of the paternal allele of melanoma antigen L2 (MAGEL2), one of five protein‐coding genes within the Prader‐Willi syndrome (PWS) critical domain. SYS…
read more here.
Keywords:
schaaf yang;
melanoma antigen;
antigen magel2;
yang syndrome ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2021 at "Clinical Genetics"
DOI: 10.1111/cge.14000
Abstract: Short stature is a common phenotype in children with Schaaf–Yang syndrome (SYS). Prader–Willi syndrome (PWS) and SYS share several phenotypic features including short stature, muscular hypotonia and developmental delay/intellectual disability. Evidence exists that similar to…
read more here.
Keywords:
rhgh therapy;
schaaf yang;
children schaaf;
therapy ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2022 at "Journal of Medical Genetics"
DOI: 10.1136/jmg-2022-108690
Abstract: Background Schaaf-Yang syndrome (SYS) is caused by truncating mutations in MAGEL2, mapping to the Prader-Willi region (15q11-q13), with an observed phenotype partially overlapping that of Prader-Willi syndrome. MAGEL2 plays a role in retrograde transport and…
read more here.
Keywords:
yang syndrome;
pathophysiology;
truncated magel2;
schaaf yang ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2022 at "Frontiers in Microbiology"
DOI: 10.3389/fmicb.2022.1007609
Abstract: The present study aims to study and analyze the characteristics of gut mucosal microbiota in diarrhea mice with deficiency kidney-yang syndrome. Ten male mice were randomly divided into the control group and the model group.…
read more here.
Keywords:
yang syndrome;
kidney;
deficiency kidney;
mucosal microbiota ... See more keywords