WordNet

relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
inflammation of many or all of the peripheral nerves (as in leprosy) (同)multiple neuritis
lacking motor coordination; marked or caused by ataxia (同)atactic

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家族の,家族特有の / 違伝的な,血統にあらわれる

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1. 家族性急性白血病および骨髄異形成症候群 familial acute leukemia and myelodysplastic syndromes
2. 家族性腺腫性ポリポーシス：患者および家族のスクリーニングおよびマネージメント familial adenomatous polyposis screening and management of patients and families
3. 家族性腺腫性ポリポーシスの臨床症状および診断 clinical manifestations and diagnosis of familial adenomatous polyposis
4. 副腎不全の稀な原因 unusual causes of adrenal insufficiency
5. 膵外分泌癌の疫学および危険因子 epidemiology and risk factors for exocrine pancreatic cancer

English Journal

[Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases].

Tanji H1, Takeda A, Tateyama M, Mochizuki H, Itoyama Y.
Rinshō shinkeigaku = Clinical neurology.Rinsho Shinkeigaku.1995 Jul;35(7):793-7.
We reported two sibling cases of progressive cerebellar ataxia accompanied with muscular atrophy of Charcot-Marie-Tooth (CMT) type. Autosomal recessive inheritance was suggested because of the parental consanguinity and other family history. The first symptom was ataxic gait in their teens, and spee
PMID 8777805

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