cleidocranial dysplasia/surdez

O link é salvo na área de transferência

ArtigosTestes clínicosPatentes

Escolha o tipo de classificação

12 resultados

Hearing loss as a presenting symptom of cleidocranial dysplasia.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

OBJECTIVE To report two cases of cleidocranial dysplasia in which hearing loss was the first presenting symptom. METHODS Retrospective case review. METHODS Two cases of cleidocranial dysplasia, a rare autosomal dominant skeletal dysplasia affecting both membranous and enchondral bone

The association of cleidocranial dysostosis with hearing loss.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Three new cases of cleidocranial dysostosis with hearing loss are reported in this paper. The significant points concerning this association are: (1) the hearing deficit is predominantly a middle ear conduction problem secondary to structural abnormalities of the ossicles; (2) there is sometimes a

Cleidocranial dysplasia with hearing loss.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Cleidocranial dysplasia is an inherited skeletal anomaly that affects primarily the skull, clavicle, and dentition, which can occur spontaneously, but most are inherited in autosomal dominant mode. The skull findings are brachycephaly, delayed or failed closure of the fontanelles, presence of open

Cleidocranial dysostosis, unilateral sensorineural hearing loss and gait disturbances: a clear-cut case of diagnostic mimicry?

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Audiological evaluation of patients with cleidocranial dysplasia (CCD)

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Objective: The description of clinical manifestation of hearing problems in cleidocranial dysplasia (CCD) remains limited and incomplete, since CCD constitutes a rare congenital disorder. The study aims to provide a complex panel analysis

[MRI of the cerebellopontine angle in patients with cleidocranial dysostosis].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

OBJECTIVE Cleidocranial dysostosis (CCD) is an autosomal dominant bone disorder in which deafness is common secondary to malformation of the middle ear structures. The study aimed at MRI evaluation of the cerebellopontine angle in 7 patients with a history of CCD--two generation spanned

Cleidocranial Dysplasia-dental Disorder Treatment and Audiology Diagnosis.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

A review of numerous case reports was made, in order to demonstrate the possibilities for treatment of dental disorders in patients with Cleidocranial dysplasia (CCD). In this paper, our own report, including a diagnosis of the effect on the auditory system, is presented. In addition to the triad of

Craniofacial and temporal bone CT findings in cleidocranial dysplasia.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Cleidocranial dysplasia (CCD) is a multistructural polyostotic genetic disorder that results from mutation of the CBFA1 gene. Hearing loss is a frequent finding in CCD. We describe the CT craniofacial findings in CCD and provide a comprehensive discussion of the CT temporal bone findings in these

A natural history of cleidocranial dysplasia.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia associated with clavicle hypoplasia and dental abnormalities. The condition is caused by mutations in the CBFA1 gene, a transcription factor that activates osteoblast differentiation. Clinical characteristics associated with

[Cleidocranial dysostosis. A review of 11 cases in five generations].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

A female who was born after a gestation of 37 weeks without incident. A caesarean was performed due to cephalopelvic disproportion. She had no clavicles, dehiscence of the sagittal suture, large anterior fontanelle and occipital prominence. A chest x-ray, abdominal and brain ultrasound and

Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

OBJECTIVE Cleidocranial dysplasia is an autosomal dominant skeletal syndrome characterized by open skull sutures and clavicular hypoplasia or aplasia. It results from mutations in the transcription factor CBFA1 required for osteoblast differentiation and normal bone formation. Therefore, mutations

Tissue-specific calibration of extracellular matrix material properties by transforming growth factor-β and Runx2 in bone is required for hearing.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Physical cues, such as extracellular matrix stiffness, direct cell differentiation and support tissue-specific function. Perturbation of these cues underlies diverse pathologies, including osteoarthritis, cardiovascular disease and cancer. However, the molecular mechanisms that establish

Junte-se à nossa
página do facebook

Herbal & Natural Medicine

O mais completo banco de dados de ervas medicinais apoiado pela ciência

Funciona em 55 idiomas
Curas herbais apoiadas pela ciência
Reconhecimento de ervas por imagem
Mapa GPS interativo - marcar ervas no local (em breve)
Leia publicações científicas relacionadas à sua pesquisa
Pesquise ervas medicinais por seus efeitos
Organize seus interesses e mantenha-se atualizado com as notícias de pesquisa, testes clínicos e patentes

Digite um sintoma ou doença e leia sobre ervas que podem ajudar, digite uma erva e veja as doenças e sintomas contra os quais ela é usada.
* Todas as informações são baseadas em pesquisas científicas publicadas