Results 81 to 90 of about 65,546 (106)

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  

Case of Monostotic Fibrous Dysplasia in the hand [PDF]

, 2002
A case of monostotic fibrous dysplasia in the proximal phalanx of an otherwise healthy, twenty-five year old is discussed. Fibrous dysplasia in the hand is rarely seen. Our patient presented with a swelling in his proximal phalanx.
Sciberras, Carmel, Zammit, Jason, Attard, Gerhardt   +2 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  

Cleidocranial dysplasia in a Moroccan patient: a case report

Cleidocranial dysplasia is a rare autosomal dominant disorder characterized by skeletal and dental anomalies, often enabling early recognition by dental practitioners.
Khadija Oumensour, Samira Elarabi, Hafsa Mansy, Jamila Ait Ikiss   +3 more
core   +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  

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  

Multiple impacted teeth in cleidocranial dysplasia: A radiographic case report

Objectives: Cleidocranial dysplasia (CCD) is an autosomal dominant malformation syndrome in which a mutation occurs in the RUNX2 gene on chromosome 6 and affects bone and tooth development. This article aims to describe the CBCT radiographic findings and
Pramanik, Farina, Epsilawati, Lusi, Hervina, Lulu   +2 more
core  

Management of cleidocranial dysplasia

Journal of the World Federation of Orthodontists, 2015
Background: This case report discusses the management of a patient diagnosed with cleidocranial dysplasia. Methods: In terms of dental characteristics, cleidocranial dysplasia features supernumerary teeth, prolonged retention of the primary teeth, and ...
Jae Hyun Park, Kiyoshi Tai
exaly   +2 more sources

Cleidocranial dysplasia with bilateral posterior glenohumeral dislocation: A case-report [PDF]

Orthopaedics and Traumatology: Surgery and Research, 2015
A 31-year-old man experienced bilateral posterior glenohumeral dislocation during seizures. He had cleidocranial dysplasia with complete absence of both clavicles.
Leroy, A., Thiong’o, M.W., Hardy, A., Laporte, C., Hardy, P.   +4 more
exaly   +2 more sources

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Molecular Genetics of Cleidocranial Dysplasia

Fetal and Pediatric Pathology, 2021
Arash Salmaninejad, Fatemeh Naqipour
exaly