A family-study with otological, neurological, and ophthalmological aspects (unilateral deafness, speech defect, dyslexia, petit mal, aphasia (Kramer-Pollnow syndrome?), astigmatism (amblyopia), disseminated sclerosis and goitre).
D000550:Amblyopia; D001037:Aphasia; D001251:Astigmatism; D004410:Dyslexia; D006042:Goiter; D006311:Hearing Disorders / Q000235:genetics*; D040941:Heredity; D006801:Humans; D009103:Multiple Sclerosis; D013060:Speech; D013064:Speech Disorders
HEARING DISORDERS/heredity