| CASE REPORT |
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| Year : 2014 | Volume
: 4
| Issue : 3 | Page : 74-76 |
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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's Building, 4th Floor, Dekweneh
Lebanon
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2231-0770.133340
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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. |
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