Literature DB >> 9863613

Genotypic/phenotypic heterogeneity of Kenny-Caffey syndrome.

M A Sabry, M Zaki, A Shaltout.   

Abstract

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Year:  1998        PMID： 9863613      PMCID： PMC1051528          DOI： 10.1136/jmg.35.12.1054-c

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.

Authors:  M A Sabry; M Zaki; S J Abul Hassan; D G Ramadan; M A Abdel Rasool; S A al Awadi; Q al Saleh
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

2.  Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.

Authors:  K Tahseen; S Khan; R Uma; R Usha; M M Al Ghanem; S A Al Awadi; T I Farag
Journal:  Am J Med Genet       Date:  1997-03-17

Review 3.  The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay--a report of six patients.

Authors:  E Hershkovitz; S Shalitin; J Levy; E Leiberman; A Weinshtock; I Varsano; R Gorodischer
Journal:  Isr J Med Sci       Date:  1995-05
  3 in total
  5 in total

1.  Craniofacioskeletal syndrome: an X-linked dominant disorder with early lethality in males.

Authors:  Roger E Stevenson; Cam K Brasington; Cindy Skinner; Richard J Simensen; J Edward Spence; Shelli Kesler; Allan L Reiss; Charles E Schwartz
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802

2.  Unusual cause of hypocalcemic seizures in a neonate.

Authors:  Pooja Dewan; Shrishail Gidaganti; M M A Faridi; Prerna Batra; Siddhnath Sudhanshu
Journal:  Indian J Pediatr       Date:  2013-12-03       Impact factor: 1.967

3.  Kenny Caffey syndrome with severe respiratory and gastrointestinal involvement: expanding the clinical phenotype.

Authors:  Loucas Christodoulou; Anil Krishnaiah; Christina Spyridou; Vincenzo Salpietro; Siobhan Hannan; Anand Saggar; Kshitij Mankad; Akash Deep; Maria Kinali
Journal:  Quant Imaging Med Surg       Date:  2015-06

4.  Neurological manifestations in children with Sanjad-Sakati syndrome.

Authors:  Ahmed Farag Elhassanien; Hesham Abdel-Aziz Alghaiaty
Journal:  Int J Gen Med       Date:  2013-05-27

5.  Kenny-Caffey syndrome type 1 in an Egyptian girl.

Authors:  Kotb Abbass Metwalley; Hekma Saad Farghaly
Journal:  Indian J Endocrinol Metab       Date:  2012-09
  5 in total

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