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Central precocious puberty 1
- ... CPP Gonadotropin-dependent precocious puberty Genetic Testing Registry: Central precocious puberty 1 Genetic Testing Registry: Precocious puberty, central, 2 National ...
- ... of a novel MKRN3 missense mutation in familial central precocious puberty. Clin Endocrinol (Oxf). 2016 Jan;84(1):80-4. doi: 10.1111/cen.12854. Epub ... maternally imprinted gene MKRN3 are common in familial central precocious puberty. Eur J Endocrinol. 2016 Jan;174(1):1-8. doi: 10.1530/EJE-15-0488. ...
- ... a hormonal problem, such as early sexual development (precocious puberty) or low levels of vitamin D (which is a hormone). PURA syndrome is a rare condition affecting at least 70 individuals. It is estimated to account for fewer than 1 percent of cases of developmental delay. PURA syndrome ...
- ... in childhood; a skin condition called eczema; early (precocious) puberty and, in females, ... syndrome is unknown. It may be as high as 1 in 5,000 individuals in the general population ...
- ... bone Albright's syndrome Albright's syndrome with precocious puberty Albright-McCune-Sternberg syndrome Albright-Sternberg syndrome Fibrous dysplasia with pigmentary skin changes and precocious puberty MAS Osteitis fibrosa disseminata PFD POFD Polyostotic fibrous ...
- ... in boys and men with familial male-limited precocious puberty. These mutations replace single protein building blocks (amino ... excess of testosterone, leading to familial male-limited precocious puberty. Affected boys begin exhibiting the signs of puberty, ...