Allgrove syndrome with features of familial dysautonomia: A novel mutation in the AAAS gene
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1080/08035250500538999/fullpdf
Reference14 articles.
1. FAMILIAL GLUCOCORTICOID DEFICIENCY WITH ACHALASIA OF THE CARDIA AND DEFICIENT TEAR PRODUCTION
2. Allgrove syndrome in adulthood
3. The "4A" syndrome: adrenocortical insufficiency associated with achalasia, alacrima, autonomic and other neurological abnormalities
4. Familial Adrenal Insufficiency, Achalasia, Alacrima, Peripheral Neuropathy, Microcephaly, Normal Plasma Very Long Chain Fatty Acids, and Normal Muscle Mitochondrial Respiratory Chain Enzymes
5. Mutant WD-repeat protein in triple-A syndrome
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