Aspartylglucosaminuria
Aspartylglucosaminuria is an autosomal recessive genetic disease caused by a deficiency of aspartylglucosaminidase in the body, characterized by mental retardation, coarse facial features, multiple bone dysplasias, vacuoles in lymphocytes in the peripheral blood, and the absence of mucopolysacchariduria.
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Site of disease:
Bone blood vessels -
Infectious :
Not contagious -
Frequent population:
All groups -
Related symptoms:
Language disorder short neck recurrent upper respiratory tract infection obvious cheek indentation recurrent upper respiratory tract infection
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Calcium Gluconate Oral Solution
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