Add to ORKGWe report a case of association between genetic haemochromatosis and mixed gonadal dysgenesis. To our knowledge, this case is the first reported in the literature. We discuss the mechanisms of hypogonadism observed in this patient
The authors report the case of two patients with secondary hemochromatosis in whom a C282Y mutation ...
A 42-year-old man developed hypogonadotropic hypogonadism due to primary hemochromatosis. Endocrine ...
The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare. We r...
Résumé L’Hémochromatose Héréditaire est. une maladie génétique qui évolue en silence. Son diagnostic...
Mixed gonadal dysgenesis (MGD) is an intersex genetic abnormality characterized by a streak gonad an...
BackgroundHereditary hemochromatosis resulting either from homozygosity for the C282Y polymorphism o...
Background: HFE-related genetic haemochromatosis (GH) is the commonest inherited genetic disorder in...
Hereditary hemochromatosis (HH) is a genetic disorder of iron overload and subsequent organ damage. ...
Objectives: Hypogonadism is defined as inadequate sex hormone production due to defects in the hypot...
Haemochromatosis (GH) is an autosomal recessive disorder in which increased iron absorption causes i...
Juvenile haemochromatosis or haemochromatosis type 2 is a rare autosomal recessive disorder which ca...
Congenital hypogonadotropic hypogonadism (CHH) is a rare disease characterized by delayed/absent pub...
International audienceThe coexistence of triple A syndrome (AAAS) and congenital hypogonadotropic hy...
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder resulting in absent puberty and in...
Congenital disorders of sex development (DSD) can be explained by exposure to harmful environmental ...
The authors report the case of two patients with secondary hemochromatosis in whom a C282Y mutation ...
A 42-year-old man developed hypogonadotropic hypogonadism due to primary hemochromatosis. Endocrine ...
The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare. We r...
Résumé L’Hémochromatose Héréditaire est. une maladie génétique qui évolue en silence. Son diagnostic...
Mixed gonadal dysgenesis (MGD) is an intersex genetic abnormality characterized by a streak gonad an...
BackgroundHereditary hemochromatosis resulting either from homozygosity for the C282Y polymorphism o...
Background: HFE-related genetic haemochromatosis (GH) is the commonest inherited genetic disorder in...
Hereditary hemochromatosis (HH) is a genetic disorder of iron overload and subsequent organ damage. ...
Objectives: Hypogonadism is defined as inadequate sex hormone production due to defects in the hypot...
Haemochromatosis (GH) is an autosomal recessive disorder in which increased iron absorption causes i...
Juvenile haemochromatosis or haemochromatosis type 2 is a rare autosomal recessive disorder which ca...
Congenital hypogonadotropic hypogonadism (CHH) is a rare disease characterized by delayed/absent pub...
International audienceThe coexistence of triple A syndrome (AAAS) and congenital hypogonadotropic hy...
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder resulting in absent puberty and in...
Congenital disorders of sex development (DSD) can be explained by exposure to harmful environmental ...
The authors report the case of two patients with secondary hemochromatosis in whom a C282Y mutation ...
A 42-year-old man developed hypogonadotropic hypogonadism due to primary hemochromatosis. Endocrine ...
The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare. We r...