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Differential Diagnosis For Prader-Willi syndrome - Rule Outs, Family history/Epilepsy

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List of current finding(s):

Metabolic, Storage Disorders
Hartnup disease
Congenital, Developmental Disorders
Sturge-Weber disease
Trichorhinophalangeal congenital synd
Hereditary, Familial, Genetic Disorders
Epilepsy, myoclonic progressive fam'ial
Tuberous Sclerosis
Laurence-Moon-Biedel syndrome
Menkes steely hair disease
Vegetative, Autonomic, Endocrine Disorders
Gilles de Tourette syndrome
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