[Cerebellar atrophy with oculocutaneous telangiectasis and bronchiectasis as a familial syndrome].
D001284:Atrophy; D001987:Bronchiectasis / Q000235:genetics*; D002526:Cerebellar Diseases; D002531:Cerebellum; D006801:Humans; D013577:Syndrome; D013684:Telangiectasis / Q000235:genetics*
BRONCHIECTASIS/genetics; CEREBELLUM/diseases; TELANGIECTASIS/genetics