References
- Djemai M, Abada-Bendib M, Masmoudi A-N, Azzôug, Chentli M. Syndrome d'Allgrove : revue de 3 familles. Revue Neurologique. 2007 April;163 (4): 112. PubMed | Google Scholar
- Brooks BP, Kleta R, Caruso RC, Stuart C, Ludlow J, Stratakis
CA. Triple A syndrome with prominent ophthalmic features and a novel mutation
in the AAAS gene:a case report. BMC Ophthalmol.2004;4:7. PubMed | Google
Scholar
- Spiegel R, Shaley S, Huebner A, Horovitz Y. Association of chronic symptomatic neutropenia with the Triple A syndrome. J Pediatr Hematol Oncol. 2005 Jan;27(1):53-5. PubMed | Google Scholar
- Aghajanzadeh M, Safarpoor F, Hydayati MH, Kohssari MR, Mashhour MY, Soleymani AS. Allgrove syndrome: reports of cases and literature. Saudi J Gastroenterol. 2006 Jan-Mar;12(1):34-5. PubMed | Google Scholar
- Kimber J, McLean BN, Prevett M, Hammans SR. Allgrove or
4 "A" syndrome: an autosomal recessive syndrome causing multisystem neurological
disease. J Neurol Neurosurg Psychiatry. 2003 May;74(5):654-7. PubMed | Google
Scholar
- Gazarian M, Cowell CT, Bonney M, Grigor WG. The "4A" syndrome:
adrenocortical insufficiency associated with achalasia, alacrima, autonomic
and other neurological abnormalities. Eur J Pediatr. 1995 Jan;154(1):18-23. PubMed | Google
Scholar
- Moore PS, Couch RM, Perry YS, Shuckett EP, Winter JS. Allgrove syndrome: An autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima. Clin Endocrinol (Oxf). 1991;34(2):107-14. PubMed | Google Scholar
- Mullaney P et al . Keratoconjunctivitis sicca associated with achalasia of the cardia, adrenalcortical insufficiency and lacrimal gland degeneration: Keratoconjunctivitis sicca secondary to lacrimal gland degeneration may parallel degenerative changes in esophageal and adrenocortical function. Ophthalmology. 1998;105(4):643-50. PubMed | Google Scholar
- Kalpana Babu, Krishna R Murthy, Narendra Babu, S Ramesh.Triple A syndrome with ophthalmic manifestations in two siblings. Indian journal of oph. 2007; 55(4):304-6. PubMed | Google Scholar
- Wanders RJ, Van Roermun CW, Schelen, A, Schutgens RBH, Zeman J, Kozich V, Hyanek J, Casteels M, Mannaerts GP.Di-and trihydroxycholestanaemia in twin sisters. J Inherit Metab Dis. 1991;14(3): 357-60. PubMed | Google Scholar
- Heinrichs C, Tsigos C, Descheppe RJ, Drews R, Collu R, Dugardeyn C, Goyens P, Ghanem GE, Bosson D, Chrousos GP et al. Familial adrenocorticotropin unresponsiveness associated with alacrima and achalasia: biochemical and molecular studies in two siblings with clinical heterogeneity. Eur J Pediatr. 1995;154(3):191-6. PubMed | Google Scholar
&