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Differential Diagnosis For Adolescent: Hereditary, Familial, Genetic Disorders

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List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Epilepsy, myoclonic progressive fam'ial
Mediterranean fever, periodic
Periodic paralysis, hypokalemic
Erb's Muscular Dystrophy/Limb Girdle MD
Gardner syndrome
Lipodystrophy/familial/dominant
Nephritis, hereditary (Alports)
Peroneal muscular atrophy(Charcot Mar.)
Peutz-Jegher's intestinal polyposis
Fechtner syndrome/FTNS (22q11.2)
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Schilder disease/Adrenoleukodystrophy
Gittleman's syndrome
Pancreatitis, hereditary
Van Bogaert encephalitis
Bartter's syndrome
Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3)
Friedreich's Ataxia
Howel-Evans syndrome
Kleine-Levin syndrome
Metaphyseal chondrodysplasia
Refsum's disease
Shwachman (Shwachman-Diamond) syndrome
Sneddon/Livedo reticularis syndrome
Segawa Syndrome/Infant Parkinsonism
Welander syndrome (See Kugelberg Welander)
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