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

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List of current finding(s):

Metabolic, Storage Disorders
Neonatal hyperbilirubinemia
Deficiency Disorders
Goiter, iodine deficiency
Congenital, Developmental Disorders
Neonatal goiter
Pendred syndrome
Hereditary, Familial, Genetic Disorders
Laurence-Moon-Biedel syndrome
Vegetative, Autonomic, Endocrine Disorders
Hyperthyroidism (Graves disease)
Hypothyroidism (myxedema)
Hypothyroidism, juvenile
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