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家族性低磷血性骨软化症是一种X染色体的显性遗传疾患,有明显家族倾向。但也有常染色体显性或隐性遗传者;也有散发病例,并无家族史。X染色体伴性显性遗传这种形式在人类较少,因而本病罕见。特别是一家系母女二
Familial hypophosphatemic osteomalacia is a dominant genetic disorder of the X chromosome with a clear family tendency. But there are also autosomal dominant or recessive genetic; also sporadic cases, there is no family history. X chromosome with dominant dominant this form less in humans, so the disease is rare. Especially a mother and daughter two