Androgen Insensitivity Syndrome in Children
Androgen insensitivity syndrome (AIS) is a common single gene sexual development disorder in children. Due to the complete or partial loss of the normal effect of androgens, it leads to a variety of clinical manifestations, ranging from a complete female phenotype to a male phenotype with only insufficient masculinization or infertility. It is the most common male pseudohermaphroditism. The disease occurs in people with a chromosome karyotype of 46, XY. In AIS, this disease is X-linked recessive inheritance and occurs in the same family.
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Site of disease:
Male reproduction Female reproduction -
Infectious :
Not contagious -
Frequent population:
Newborns (less than one month old) -
Related symptoms:
Labia fusion Secondary amenorrhea Gonadal dysplasia Breast dysplasia No axillary hair
Related Drugs
Recombinant human growth hormone injection
Indication: Used for slow growth in children caused by endogenous growth hormone deficiency; for the treatment of severe burns; for growth hormone deficiency caused by established hypothalamic-pituitary disease and significant growth hormone deficiency confirmed by two different growth hormone stimulation tests.
Recombinant human growth hormone injection
Indication: Used for slow growth in children caused by endogenous growth hormone deficiency; for the treatment of severe burns; for growth hormone deficiency caused by established hypothalamic-pituitary disease and significant growth hormone deficiency confirmed by two different growth hormone stimulation tests.
Related Ingredients
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Somatonorm list
82030-87-3