Results 81 to 90 of about 72,220 (148)

Cleidocranial dysplasia: a dilemma in diagnosis?

, 2010
Cleidocranial dysplasia is a developmental anomaly and is characterized by craniofacial and skeletal malformations as well as the presence of numerous supernumerary and unerupted teeth.
Husna Zayadi
core  

Disostosis cleido-craneal: Estudio clínico, radiográfico y genético de una familia

Revista Cubana de Medicina, 1999
Se presentó un estudio clínico, radiográfico y el árbol genealógico de una familia afectada de disostosis cleido-craneal realizado en el Hospital Clinicoquirúrgico "Celia Sánchez Manduley" de la ciudad de Manzanillo, en 1998.
César Mustelier Fernández, Marlenes Chang Lago, Arturo Luis Almunia Leyva, Mireille Molero Segrera   +3 more
doaj  

Persistent or large anterior fontanel associated with hypermobility of the shoulders - Cleidocranial dysplasia?

, 2005
This article discusses two non-related children, who presented at an age of 20 and 1.5 months respectively with a persistent or large anterior fontanel associated with hypermobility of the shoulders.
Terhal, P. A., Cohen, J., De Waal, W. J., Hagendoorn, J., dLAB Biobank, MS CGO, Child Health, Genetica Klinische Genetica, Giltay, J., Cancer   +9 more
core  

Cleidocranial Dysplasia: A Rare Cause of Disproportionate Severe Short Stature

Oman Medical Journal, 2012
Skeletal dysplasia is an uncommon cause of short stature in children. An 11-year-old girl was evaluated for severe short stature in a tertiarycare hospital.
Manzoor Ahmad Bhat, Bashir Ahmad Laway, Suhail Mantoo, Khalid Choudry, Suman Kotwal, Shahnaz Ahmad Mir   +5 more
doaj  

6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing

, 2013
[[abstract]]We present an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay, poor wound healing and a 6p21.2–p12.3 deletion detected by aCGH.
陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Liu, Yu-Peng;Liu, Yu-Peng;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Su, Jun-Wei;Su, Jun-Wei;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen
core  

A Clinical Odyssey Involving Cleidocranial Dysplasia: Report of a Rare Case. [PDF]

Cureus, 2023
Agarwal N, Daigavane P, Kamble R, Suchak D.   +3 more
europepmc   +1 more source

Yunis Varon Syndrome

Online Journal of Health & Allied Sciences, 2010
We have reported a case of Yunis-Varon syndrome which is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones, characteristic facial features, abnormalities of the fingers and/or toes ...
Sameer I. Dal, Parin Parmar
doaj  

Cleidocranial dysplasia with complex oral manifestations: a case report. [PDF]

BMC Oral Health
Çitaku E, Çitaku E, Reshitaj A.
europepmc   +1 more source

Cleidocranial dysplasia

, 2001
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower segment: 0.9:1), macrocephaly (head circumference 59.5cm), brachycephaly and prominent forehead.
S. Gulati, M. Kabra
core   +1 more source

Cleidocranial dysplasia with preserved function under conservative management: a case report. [PDF]

Front Pediatr
Xu H, Ma J, Huang X, Pu S, Hou F, Liu W, Chen J.   +6 more
europepmc   +1 more source