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Kallmann syndrome 1
- Kallmann syndrome is a condition characterized by delayed or absent puberty and an impaired sense of smell.This disorder is a form of hypogonadotropic hypogonadism, ...
- ... ANOS1 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... 5 to 10 percent of all cases of Kallmann syndrome.The ANOS1 gene mutations that cause Kallmann syndrome ...
- ... 30 mutations in the PROKR2 gene can cause Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 9 percent of all cases of Kallmann syndrome.Most of the PROKR2 gene mutations that cause ...
- ... FGFR1 gene variants have been found to cause Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 10 percent of all cases of Kallmann syndrome. The FGFR1 gene variants that cause Kallmann syndrome ...
- ... CHD7 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... 5 to 10 percent of all cases of Kallmann syndrome.Many people with Kallmann syndrome caused by a ...
- ... PROK2 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 9 percent of all cases of Kallmann syndrome.Most of the PROK2 gene mutations that cause ...
- ... FGF8 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for a small percentage of all cases of Kallmann syndrome.Most of the FGF8 gene mutations that cause ...
- ... This Health Condition MedlinePlus Genetics provides information about Kallmann syndrome More About This Health Condition DOM dominant megacolon, ...
- ... vocal cords; and a set of symptoms called Kallmann syndrome, which features delayed or absent puberty and an ...