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
a sudden uncontrollable attack; "a paroxysm of giggling"; "a fit of coughing"; "convulsions of laughter" (同)fit, convulsion
accompanied by or of the nature of paroxysms

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1. 高リン血症の原因および治療の概要 overview of the causes and treatment of hyperphosphatemia
2. 横紋筋融解症の原因 causes of rhabdomyolysis
3. 筋力低下を呈する小児の病因および評価 etiology and evaluation of the child with muscle weakness
4. 高カルシウム血症の原因 etiology of hypercalcemia
5. ヘム色素誘発急性腎障害（急性腎不全）の臨床的特徴および診断 clinical features and diagnosis of heme pigment induced acute kidney injury acute renal failure

Familial paroxysmal rhabdomyolysis: management of two cases of the non-exertional type.

Ramesh V1, Gardner-Medwin D.
Developmental medicine and child neurology.Dev Med Child Neurol.1992 Jan;34(1):73-9.
Familial paroxysmal rhabdomyolysis with myoglobinuria is a rare and life-threatening disease of young children, of unknown aetiology. Attacks bear no relation to exercise, are usually triggered by intercurrent infections and are often severe. The authors describe two cases and suggest plans for the
PMID 1544519

Gullotta F, Spiess-Kiefer C.
Fortschritte der Neurologie-Psychiatrie.Fortschr Neurol Psychiatr.1983 Oct;51(10):355-8.
Rhabdomyolysis can appear secondarily in the course of many different diseases, but also primarily as "idiopathic paroxysmal rhabdomyolysis" (i.p.r.), simulating clinically an acute myositis. Different factors can trigger this muscle reaction, the most important of them being physical stress, alcoho
PMID 6642396

Gullotta F, Spiess-Kiefer C.
Anästhesie, Intensivtherapie, Notfallmedizin.Anasth Intensivther Notfallmed.1983 Feb;18(1):21-7.
Muscle biopsies were carried out in 41 patients with malignant hyperthermia, or supposed at-risk, as well as in some of their relatives. In 20 patients no changes were detected, and in 2 patients only acute rhabdomyolysis was seen (53.7%); in 19 patients (that is 46.3%) myopathic aspects were found
PMID 6846753