Results 51 to 60 of about 65,546 (106)

CLEIDOCRANIAL DYSPLASIA, NEUROFIBROMATOSIS TYPE-I WITH FRONTAL LOBE GLIOMA

Pakistan Armed Forces Medical Journal, 2005
Introduction Cleidocranial Dysplasia is a benign hereditary condition, inherited as an autosomal dominant. The disease has considerable variation of expression. Thirty percent of the cases are due to spontaneous mutation [1]. The gene responsible for
Muhammad Nazir, Asim Rafiq
doaj   +2 more sources

MECP2 Insufficiency Attenuates RUNX2‐Dependent Osteoblast Differentiation via miR‐126‐3p/DKK1‐Mediated Canonical Wnt Signaling Inhibition in Rett Syndrome

The FASEB Journal, Volume 40, Issue 4, 28 February 2026.
MECP2 insufficiency leads to upregulation of miR‐126‐3p, which in turn enhances the endogenous Wnt antagonist DKK1. DKK1 inhibits the canonical Wnt signaling pathway, thereby impairing RUNX2‐dependent osteoblast differentiation. ABSTRACT Rett syndrome (RTT) is a rare neurodevelopmental disorder caused by loss‐of‐function mutations in the gene encoding ...
Shuangshan Dong, Lu Wang, Hiroki Kato, Saki Hirofuji, Zhiyan Zhou, Yosuke Ito, Yuta Hirofuji, Hiroshi Sato, Takahiro A. Kato, Yasunari Sakai, Shouichi Ohga, Satoshi Fukumoto, Keiji Masuda   +12 more
wiley   +1 more source

Tissue-specific calibration of extracellular matrix material properties by transforming growth factor-beta and Runx2 in bone is required for hearing [PDF]

, 2010
Publisher version: http://www.nature.com/embor/journal/v11/n10/full/embor2010135.htmlDA - 20100917 IS - 1469-3178 (Electronic) IS - 1469-221X (Linking) LA - ENG PT - JOURNAL ARTICLEDA - 20100917 IS - 1469-3178 (Electronic) IS - 1469-221X (Linking) LA ...
Anil Lalwani, Chin, EN, Carol G Chen, Derynck, R, Marshall, GW, Butcher, K, Guive Balooch, Lawrence Lustig, Akil, O, Porter, AE, Robert O Ritchie, Grayson W Marshall, Jacob Johnson, Lalwani, A, Sally J Marshall, Omar Akil, Emily N Chin, Balooch, G, Humphrey, MB, Lustig, L, Delia S Brauer, Rik Derynck, Kristin Butcher, Marshall, SJ, Richard A Schneider, Tamara Alliston, Alliston, T, Chen, CG, Johnson, J, Jolie L Chang, Brauer, DS, Alexandra E Porter, Schneider, RA, Chang, JL, Ritchie, RO, Mary Beth Humphrey   +35 more
core   +1 more source

The Metacarpophalangeal Pattern Profile: An Old Method With New Insights Into the Evaluation of Short Stature

American Journal of Human Biology, Volume 38, Issue 2, February 2026.
ABSTRACT Objective To characterize the metacarpophalangeal pattern profile (MCPP) of healthy children and adolescents from São Paulo, Brazil, and to establish percentile curves by chronological age (CA), bone age (BA), and sex using the LMS method. Additionally, to compare these findings with previous population‐based data and to apply the derived ...
Marcelo Damaso Maruichi, Bruno Telma Destailleur, Giulia Maesta Apelbaum, Carlos Alberto Longui, Cristiane Kochi   +4 more
wiley   +1 more source

A Rare Case Report of Four Bilateral Maxillary Lateral Incisors in a Non‐Syndromic Patient

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Bilateral supernumerary maxillary lateral incisors in non‐syndromic adults are extremely rare and pose diagnostic and treatment challenges. This case report describes a 34‐year‐old male with esthetic concerns and malocclusion, successfully managed through strategic extraction, transverse expansion, and fixed orthodontic therapy, achieving ...
Seyed‐Mohsen Hosseini‐Adib, Mona Kazemi   +1 more
wiley   +1 more source

Sequential Double Autotransplantation Using Immature Teeth as First‐Stage Autotransplants to Preserve Alveolar Architecture: A Case Series

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Introduction Missing teeth in growing patients require treatment approaches that preserve alveolar bone and support continued development. Autotransplantation offers a biological alternative to implants, yet severely compromised recipient sites and immature donor teeth present clinical challenges.
Miks Lejnieks, Juan E. Onetto, Marie-Therese Flores, Andris Abeltins, Girts Salms, Sergio E. Uribe, Hannah Wesley   +6 more
wiley   +1 more source

Pediatric Dental Management of a Patient With Infantile Osteopetrosis in Remission: A Clinical Case Report

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Background Osteopetrosis is a rare genetic disorder characterized by increased bone density due to defective osteoclast function. Its clinical presentation varies according to subtype, and oral manifestations are frequent, potentially serving as early indicators of the disease.
Maria Amalia Cruz-Morera, Katherine Molina-Chaves, Adrian Gomez-Fernandez, Hannah Wesley   +3 more
wiley   +1 more source

Cleidocranial Dysplasia – A Late Diagnosis

, 2006
Cleidocranial dysplasia is a rare congenital disorder of bone characterized by abnormalities of clavicle, skull and dentition. There are features which are pathognomic for this condition and diagnosis can usually be made early in life.
Suresh Nayar, Karl Bishop
core   +1 more source

Pycnodysostosis Unveiled: Craniofacial and Dental Manifestations in Focus

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Pycnodysostosis refers to an uncommon autosomal recessive developmental anomaly, which results in decreased bone remodeling, manifesting itself in a variety of clinical and radiographic displays. We report two cases involving two sisters aged 12.5 and 8 years old from a consanguineous marriage.
Khaoula M′Rabt, Soufiane Kharraz, Hind Ramdi, Fatima Zaoui, Abdelali Halimi, Hannah Wesley   +5 more
wiley   +1 more source

Orthognathic Surgery in Patients With Cleidocranial Dysplasia

, 2015
The aim of this study was to report the orthodontic-surgical approach of a 21-year-old female patient diagnosed with cleidocranial dysplasia. An orthognathic surgery was performed in the maxilla and mandible during the same procedure to correct an ...
Dias-Ribeiro, Eduardo, Sonoda, Celso Koogi, Caetano, Isabela Maria, Rocha, Julierme Ferreira [UNESP], Sant'Ana, Eduardo, Rocha, Julierme Ferreira, Dias-Ribeiro, Eduardo [UNESP], Faria Yaedu, Renato Yassutaka, Conceicao Madeira, Maria Fernanda, Sonoda, Celso Koogi [UNESP]   +9 more
core   +1 more source