Familial Hypopituitarism
What's New
Last Posted: Jan 01, 2011
- Familial hypopituitarism
From NCATS Genetic and Rare Diseases Information Center - HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
McNay David E G, et al. The Journal of clinical endocrinology and metabolism 2007 2 (2) 691-7
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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