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X-linked adrenal hypoplasia congenita
・ X-linked agammaglobulinemia
・ X-linked congenital stationary night blindness
・ X-linked dominant inheritance
・ X-linked endothelial corneal dystrophy
・ X-linked hypertrichosis
・ X-linked hypophosphatemia
・ X-linked ichthyosis
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・ X-linked recessive hypoparathyroidism
・ X-linked recessive inheritance
・ X-linked reticulate pigmentary disorder


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X-linked adrenal hypoplasia congenita : ウィキペディア英語版
X-linked adrenal hypoplasia congenita

X-linked adrenal hypoplasia congenita is a genetic disorder that mainly affects males. It involves many endocrine tissues in the body, especially the adrenal glands.
==Presentation==
One of the main characteristics of this disorder is adrenal insufficiency, which is a reduction in adrenal gland function resulting from incomplete development of the gland's outer layer (the adrenal cortex). Adrenal insufficiency typically begins in infancy or in childhood and can cause vomiting, difficulty with feeding, dehydration, extremely low blood sugar (hypoglycemia), low sodium levels, and shock. However, adult-onset cases have also been described. See also Addison's Disease.
Affected males may also lack male sex hormones, which leads to underdeveloped reproductive tissues, undescended testicles (cryptorchidism), delayed puberty, and an inability to father children (infertility). These characteristics are known as hypogonadotropic hypogonadism. Females are rarely affected by this disorder, but a few cases have been reported of adrenal insufficiency or a lack of female sex hormones, resulting in underdeveloped reproductive tissues, delayed puberty, and an absence of menstruation.

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