تظاهرات سندرم آلگرو (Allgrove Syndrome) بدنبال اسهال و استفراغ

Authors

  • طایی, نادره گروه اطفال، دانشکده پزشکی، دانشگاه علوم پزشکی لرستان
  • طرهانی, فریبا گروه اطفال، دانشکده پزشکی، دانشگاه علوم پزشکی لرستان
  • عباسی, فرزانه گروه غدد و متابولیک اطفال، بیمارستان شریعتی، دانشگاه علوم پزشکی تهران
Abstract:

Allgrove (AAA) syndrome or familial glucocorticoid deficiency or Tripple A Syndrome is a rare genetic disorder with transmitted autosomal recessive. Allgrove and colleagues first described this syndrome in 1978. Allgrove Syndrome characterized by Adrenal insufficiency, Alacrima and Achalasia. Neurological and dermatological findings may be presented in some patients. Hyperpigmentation and Alacrima are diagnostic key findings in Allgrove Syndrome. In this report we describe a 2 year old patient with the clinical picture of Allgrove Syndrome after gasteroenteritis.

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Journal title

volume 13  issue None

pages  105- 111

publication date 2011-08

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