Answer;
-Prader-Willi syndrome
Explanation:
-Prader-Willi syndrome (PWS) is a disorder caused by a deletion or disruption of genes in the proximal arm of chromosome 15 or by maternal disomy in the proximal arm of chromosome 15.
-The commonly associated characteristics of this disorder include diminished fetal activity, obesity, hypotonia, short stature, hypogonadotropic hypogonadism, strabismus, and small hands and feet.