Kenny-Caffey syndrome type 1
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.
Saved in:
| Main Authors: | , , , , |
|---|---|
| Format: | article |
| Language: | EN |
| Published: |
Thieme Medical and Scientific Publishers Pvt. Ltd.
2014
|
| Subjects: | |
| Online Access: | https://doaj.org/article/ea2f9fb7c58148009571390a3fa3e3a0 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|