نتایج جستجو برای: cleidocranial dysplasia

تعداد نتایج: 28648  

Journal: :Developmental Dynamics 1997

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Journal: :Nosotchu 2018

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Journal: :Oral health and dental management 2014
U Romeo G Galluccio G Palaia G Tenore F Carpenteri E Barbato A Polimeni

INTRODUCTION Cleidocranial Dysplasia (CCD) is a rare inherited autosomal dominant congenital syndrome that occurs in approximately one out of every one million individuals worldwide; it primarily affects bones that undergo intra-membranous ossification, generally the skull and clavicles. Other bones may be affected such as the long bones, spine, pelvis, bones of hands and feet showing hypoplasi...

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2014
Maria Felicia Faienza Annamaria Ventura Laura Piacente Maria Ciccarelli Margherita Gigante Loreto Gesualdo Silvia Colucci Luciano Cavallo Maria Grano Giacomina Brunetti

Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia characterized by hypoplastic or aplastic clavicles, dental abnormalities, and delayed closure of the cranial sutures. In addition, mid-face hypoplasia, short stature, skeletal anomalies and osteoporosis are common. We aimed to evaluate osteoclastogenesis in a child (4 years old), who presented with clinical signs of CCD a...

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Journal: :Middle East journal of anaesthesiology 2012
Cindy Jessica Wang Steven Mark Neustein

Cleidocranial dysplasia (CD) is a rare disorder that involves developmental abnormalities of bony structures. CD is characterized as an autosomal dominant skeletal dysplasia with a variety of clinical manifestations; most commonly supernumerary teeth, brachycephalic skull, short stature, and hypoplastic or aplastic clavicles. In a systematic review of a study population comparing CD individuals...

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Journal: :Oman medical journal 2012
Manzoor Ahmad Bhat Bashir Ahmad Laway Suhail Mantoo Khalid Choudry Suman Kotwal Shahnaz Ahmad Mir

Skeletal dysplasia is an uncommon cause of short stature in children. An 11-year-old girl was evaluated for severe short stature in a tertiary care hospital. Clinical examination revealed severe disproportionate short stature and classical triad of multiple supernumerary teeth, and complete absence of clavicles and open sagittal sutures and fontanelles. Skeletal survey confirmed these findings,...

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Journal: :Human Mutation 2003

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Journal: :Orthodontic Forum 2020

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Journal: :BMJ Case Reports 2015

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Journal: :Case Reports in Dentistry 2020

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