Search

everythingexperts & clinicslearnfaqsresearchcommunity

for

Search:↓

This article discusses sexual interests and behavior in individuals with Prader-Willi syndrome and notes the lack of prior descriptions in this area, but reports no new clinical results.

In this case study, mosaic maternal uniparental disomy of chromosome 15 was identified as the cause of Prader–Willi syndrome in a patient through combined genetic analyses, emphasizing that mosaicism might lead to missed diagnoses if only blood tests are used.

This article reviews current knowledge and research gaps on growth hormone in hair follicle biology, highlighting its complex role and suggesting further exploration to reveal nonclassical skin functions.

This study suggests that behavior modification, semistarvation ketogenic regimens, and surgical therapy could be experimental approaches for different degrees of obesity, with their efficacy varying by the degree of weight excess.

This study developed a detailed classification system for functional androgenization in females that may enhance diagnosis and personalized treatment by identifying individual dysfunctions.