Variant arabe du syndrome de Kenny : à propos d’une famille maghrébine-Reference-Cited by-同舟云学术

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Variant arabe du syndrome de Kenny : à propos d’une famille maghrébine

Published:2005-09 Issue:4 Volume:66 Page:361-364
ISSN:0003-4266
Container-title:Annales d'Endocrinologie
language:fr
Short-container-title:Annales d'Endocrinologie

Author:

Fitouri Z.,Fayech C.,Ferchichi M.,Ben Becher S.

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Reference13 articles.

1. The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies;Al Gazali;Clin dysmorph,1997

2. Levin DB, streeten BW. Ocular finding in Kenny's syndrom;Boynton;Arch Ophtalmol,1979

3. Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic;Diaz;Am J Med Genet,1999

4. Kenny syndrome : evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one;Fanconi;J. Pediatr,1986

5. Medullary stenosis of the tubular bones associated with hypocalcemic convulsions and short stature;Frech;Radiology,1968

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