11 pages matching Waardenburg's syndrome in this book
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The A-Z Reference Book of Syndromes and Inherited Disorders
No preview available - 1996
abnormalities achondroplasia adequate adult advice Aims and provisions Antenatal diagnosis assessment associated ataxia autosomal dominant autosomal recessive baby's Batten's disease become behaviour birth blood body bones boys and girls brain cardiac CAUSATION cause CHARACTERISTICS child childhood chorionic villus sampling chromosome clinical condition cystic fibrosis deafness developmental difficulties disease disorder Down's syndrome drugs Duchenne muscular dystrophy Edward's syndrome enzyme example excess facial features feeding frequently FUTURE gene Genetic counselling give rise growth haemophilia he/she hearing Heart defects his/her Hunter's syndrome important incidence infection joints kidney learning disability MANAGEMENT IMPLICATIONS metabolic mode of inheritance muscles necessary Noonan's syndrome normal occur parents possible Prader-Willi pregnancy present problems renal respiratory result retinal Reye's syndrome seen SELF-HELP GROUP severely affected short stature skin specific speech sufferers syndrome ALTERNATIVE NAMES therapy thought tissue treatment Turner's syndrome unusual usually vision visual Waardenburg's syndrome X-linked