Pediatric Alstrom syndrome

Pediatric Alstrom syndrome is an autosomal recessive genetic disease, mainly including vision loss, neurological hearing loss, obesity, diabetes, diabetes insipidus, renal insufficiency, hypogonadism, hyperuricemia, and hypertriglyceridemia, etc. . It is the earliest and most severe inherited retinopathy, and the cone cone cell function of both eyes is completely lost at birth or within one year after birth, resulting in congenital blindness in infants and young children. Pediatric Alstrom syndrome is also known as congenital dark Mongolia, hereditary congenital retinopathy, Alstrom-Olsen syndrome and so on.

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