CLEIDOCRANIAL DYSPLASIA SYNDROME IN A NEWBORN

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EGHBALIAN F.

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Journal Paper

Paper Information

Journal: Koomesh Year:2005 | Volume:6 | Issue:3 Page(s): 251-254

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Information Journal Paper

Title

CLEIDOCRANIAL DYSPLASIA SYNDROME IN A NEWBORN

Author(s)

EGHBALIAN F. | Issue Writer Certificate

Keywords

CLAVICULAR HYPOPLASIAQ4

CLEIDOCRANIAL DYSPLASIAQ4

LARGE FONTANELQ4

Abstract

Cleidocranial dysplasia is a rare congenital bone formation inherited as an autosomal dominant trait. The incidence is one per 200000 live births. Major symptoms include delayed ossification of the skull, excessively LARGE FONTANELs and CLAVICULAR HYPOPLASIA or aplasia, allowing the shoulders in front of the chest. Delayed eruption of teeth, high arched palate and wide pelvic joint may also be present. The case was a newborn boy who had admitted in neonatal ward of Ekbatan hospital because of respiratory distress. Anterior and posterior fontanels were completely large and connected.-His shoulders were a little depressed. Chest X ray revealed bilateral clavicular agenesia and skull X-ray failed to demonstrat vortex bone.

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APA: Copy

EGHBALIAN, F.. (2005). CLEIDOCRANIAL DYSPLASIA SYNDROME IN A NEWBORN. KOOMESH, 6(3), 251-254. SID. https://sid.ir/paper/37413/en

Vancouver: Copy

EGHBALIAN F.. CLEIDOCRANIAL DYSPLASIA SYNDROME IN A NEWBORN. KOOMESH[Internet]. 2005;6(3):251-254. Available from: https://sid.ir/paper/37413/en

IEEE: Copy

F. EGHBALIAN, “CLEIDOCRANIAL DYSPLASIA SYNDROME IN A NEWBORN,” KOOMESH, vol. 6, no. 3, pp. 251–254, 2005, [Online]. Available: https://sid.ir/paper/37413/en

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