hrp0095p1-120 | Growth and Syndromes | ESPE2022
Westra D.
, Rinne T.K.
, Oud M.S.
, Ruiterkamp-Versteeg M.H.A.
, de Leeuw N.
, van der Velden A.A.E.M.
, Kempers M.J.E.
The phenotype in male individuals with a mosaic sex chromosomal abnormality is heterogenous, but ambiguous genitalia, delayed puberty, disturbed spermatogenesis, and short stature are frequently seen. Genetic investigation in boys with idiopathic/isolated short stature usually includes SHOX gene analysis (sequencing and copy number detection by MLPA), genome wide array analysis, and/or whole exome sequencing (WES). In the Netherlands, conventional karyotyping is not part of th...