نتایج جستجو برای: allgrove syndrome

تعداد نتایج: 621917  

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2016
Sommayya Aftab Jaida Manzoor Nabila Talat Hafiz Sajid Khan Maroof Subhanie Nauman Abbas Khalid

Allgrove syndrome or triple-Asyndrome is a rare familial multisystem autosomal recessive disorder. It is characterised by triad of alacrima, achalasia and adrenal insufficiency due to adrenocorticotropin hormone (ACTH) resistance. If it is associated with autonomic dysfunction, it is termed as 4-Asyndrome. This syndrome is caused by a mutation in the Achalasia - Addisonism - Alacrima (AAAS) gen...

Journal: :Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2005
Lalit Bharadia Mukesh Kalla S K Sharma Rohit Charan J B Gupta Firoz Khan

Triple A syndrome (Allgrove syndrome) is an autosomal recessive disorder consisting of achalasia, alacrima and Addison insufficiency. We report an 11-year-old girl with predominant symptom of achalasia who was diagnosed as Triple A syndrome almost 3 years after initial presentation.

Journal: :گوارش 0
ahmad khodadad mehri najafi-sani fatemeh famouri v modaresi

allgrove syndrome also known as triple-a syndrome is an autosomal recessive disorder characterized by alacremia, achalasia and acth-resistant adrenal insufficiency. although this syndrome is rare, herein we report four cases with different clinical manifestations. they were referred to the gastrointestinal ward during a one year period with complaints of vomiting and dysphagia. the diagnosis of...

Journal: :Neurology International 2018

Journal: :gastroenterology and hepatology from bed to bench 0
baran parhizkar md nakisa maghsoodi mojgan forootan amirhosein entezari

triple a syndrome (allgrove syndrome) is a rare inherited autosomal recessive disease with a typical triad including adrenocorticotrophic-hormone-resistant glucocorticoid insufficiency, reduced or absent tearing (alacrima) and achalasia and a wide range of symptoms can be detected due to multi organ involvement. this report describes the case of a triple asyndrome, a12 year-old boy with a histo...

2016
Amar Tebaibia Mohammed Amine Boudjella Djamel Boutarene Farouk Benmediouni Hakim Brahimi Nadia Oumnia

AIM To investigate the incidence of achalasia in Algeria and to determine its clinical and para-clinical profile. To evaluate the impact of continuing medical education (CME) on the incidence of this disease. METHODS From 1990 to 2014, 1256 patients with achalasia were enrolled in this prospective study. A campaign of CME on diagnosis involving different regions of the country was conducted b...

2012
Baran Parhizkar Nakisa Maghsoodi Mojgan Forootan Amir Hosein Entezari

Triple A syndrome (Allgrove syndrome) is a rare inherited autosomal recessive disease with a typical triad including adrenocorticotrophic-hormone-resistant glucocorticoid insufficiency, reduced or absent tearing (alacrima) and achalasia and a wide range of symptoms can be detected due to multi organ involvement. This report describes the case of a Triple Asyndrome, a12 year-old boy with a histo...

Journal: :The Medical journal of Australia 2004
Clarissa C Pedreira Margaret R Zacharin

We report a man with longstanding undiagnosed adrenal insufficiency. At 37, our patient is the oldest reported case. Although most cases of Allgrove syndrome are diagnosed during childhood, awareness of this condition when undiagnosed in adults is crucial, as it is life threatening, and can severely affect neurological, sexual and psychological function.

Journal: :International Journal of Clinical Case Reports 2016

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