Avicenna Journal of Medicine

CASE REPORT
Year
: 2014  |  Volume : 4  |  Issue : 3  |  Page : 74--76

Kenny-Caffey syndrome type 1


Tony El Jabbour1, Tarek Aboursheid2, Mohammad Baraa Keifo2,  Ismael Maksoud3, Diana Alasmar4 
1 Department of Anatomic Pathology, Faculty of Medicine, Lebanese University, Lebanon, Lebanon
2 Department of Pediatrics, Faculty of Medicine, Damascus, Syria
3 Pediatrics University Hospital, Damascus, Syria
4 Pediatric Endocrinology and Metabolic Diseases Unit, University Children Hospital, Faculty of Medicine, Damascus University, Damascus, Syria

Correspondence Address:
Tony El Jabbour
Saint Elie Street, Joseph Attieh«SQ»s Building, 4th Floor, Dekweneh
Lebanon

Kenny-Caffey syndrome type 1 is a rare hereditary skeletal disorder. We present here a documented case of a 7-month-old girl with the characteristic symptoms of growth retardation, dysmorphic features, and hypoparathyroidism.


How to cite this article:
El Jabbour T, Aboursheid T, Keifo MB, Maksoud &, Alasmar D. Kenny-Caffey syndrome type 1.Avicenna J Med 2014;4:74-76


How to cite this URL:
El Jabbour T, Aboursheid T, Keifo MB, Maksoud &, Alasmar D. Kenny-Caffey syndrome type 1. Avicenna J Med [serial online] 2014 [cited 2019 Sep 16 ];4:74-76
Available from: http://www.avicennajmed.com/article.asp?issn=2231-0770;year=2014;volume=4;issue=3;spage=74;epage=76;aulast=El;type=0