نتایج جستجو برای: achalasia alacrima

تعداد نتایج: 2100  

2017
Hiren Patt Katrin Koehler Sailesh Lodha Swati Jadhav Chaitanya Yerawar Angela Huebner Kunal Thakkar Sneha Arya Sandhya Nair Manjunath Goroshi Hosahithlu Ganesh Vijaya Sarathi Anurag Lila Tushar Bandgar Nalini Shah

OBJECTIVE To study genotype-phenotype spectrum of triple A syndrome (TAS). METHODS Retrospective chart analysis of Indian TAS patients (cohort 1, n = 8) and review of genotyped TAS cases reported in world literature (cohort 2, n = 133, 68 publications). RESULTS Median age at presentation was 4.75 years (range: 4-10) and 5 years (range: 1-42) for cohorts 1 and 2, respectively. Alacrima, adre...

2003
J Kimber B N McLean M Prevett S R Hammans

Allgrove’s or “4 A” syndrome is a rare autosomal recessive condition with alacrima, achalasia, autonomic disturbance, and ACTH insensitivity among other features. Recent studies have identified mutations in the AAAS, a candidate gene on chromosome 12q13 in such patients. Manifestations in adult patients are rarely reported. The syndrome usually presents during the first decade of life with dysp...

Journal: :European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry 2015
G Tadini F Besagni M Callea M Brena L C Rossi F Angiero R Crippa

BACKGROUND Triple A or Allgrove Syndrome (OMIM#231550) is a rare, autosomal recessive genetic disorder in which patients typically suffer from chronic adrenal insufficiency due to resistance to ACTH (Addison's disease), esophageal achalasia, and defective tear formation (alacrima). The syndrome is caused by mutations in the AAAS gene on chromosome 12q13 encoding a 546 aminoacid protein named al...

2012
Satoru Ikemoto Ken Sakurai Naruo Kuwashima Yoshihiro Saito Ichiro Miyata Noriyuki Katsumata Hiroyuki Ida

Allgrove syndrome, also known as triple A syndrome (OMIM #231550), is a rare autosomal recessive disorder characterized by the triad of adrenocorticotropic hormone (ACTH)-resistant adrenal insufficiency, achalasia and alacrima. It is caused by mutations of the AAAS gene, which is located on chromosome 12q13, encoding the WD-repeat protein ALADIN (alacrimaachalasia-adrenal insufficiency neurolog...

Journal: :Journal of Neurogastroenterology and Motility 2011

Journal: :Neuroscience 2005
H L Storr A J L Clark J V Priestley G J Michael

Triple A syndrome is characterised by achalasia, alacrima, adrenocorticotropin-resistant adrenal insufficiency and a variable and progressive neurological phenotype. It is caused by mutations in a gene that is normally referred to as the triple A syndrome gene (AAAS) and which has recently been shown to encode a nuclear pore protein named ALADIN (alacrima, achalasia, adrenal insufficiency neuro...

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