Zeitschrift fur Kinderheilkunde · 1975
Fanconi's anemia. I. Case histories, clinical and laboratory findings in six affected siblings.
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Prindull G, Stubbe P, Kratzer W
Аннотация
This is a study of the largest family with Fanconi's anemia known in the world literature, namely of 6 affected siblings. All patients showed the typical features of the disease, including pancytopenia, skeletal and kidney deformities, hyperpigmentation of the skin, and physical as well as mental retardation. Four of the patients have died of their disease, the 2 patients who are still living at present have a deteriorating clinical course. Case histories, clinical and laboratory findings are reported here. In the second and third part of this study [48, 52] endocrinologic and genetic findings will be reported.
Предметные рубрики MeSH
Abnormalities, MultipleAdolescentAnemia, AplasticBirth WeightBlood Cell CountBody ConstitutionBone Diseases, DevelopmentalChildChild, PreschoolEarErythrocytesFanconi AnemiaFemaleHemoglobinsHumansInfantInfant, NewbornIntellectual DisabilityLymphocyte ActivationMaleMicrophthalmosPedigreePigmentation DisordersUrogenital Abnormalities