نتایج جستجو برای: Albright syndrome

تعداد نتایج: 622258  

Journal: :international journal of pediatrics 0
moein mobini department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. rahim vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. saba vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran.

mccune-albright syndrome (mas) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. the disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  we describe a girl patient with mas having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. clinical presentat...

2015
Rita Lourenço Patrícia Dias Raquel Gouveia Ana Berta Sousa Graça Oliveira

INTRODUCTION McCune-Albright syndrome is a rare sporadic disease characterized by fibrous bone dysplasia, café-au-lait skin spots and variable hyperfunctional endocrinopathies. McCune-Albright syndrome is caused by somatic postzygotic activating mutations in the GNAS gene that produce a broad spectrum of effects. CASE PRESENTATION We report a case of McCune-Albright syndrome with multi-organ ...

2016
Se Hee Kang Ji Seon Jeong S. H. Kang J. S. Jeong

The McCune-Albright syndrome is rare disease diagnosed by the clinical triad, fibrous dysplasia, café-au lait skin pigmentations and endocrine hyperfunction. Those patients with bone issues could have various surgeries under general anesthesia. Airway abnormality and various endocrine abnormalities should be considered during general anesthesia for McCune-Albright syndrome patients. A 15-year-o...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Revista espanola de estomatologia 1984
K Triantafillidou K Antoniades D Karakasis I Rousso A Drevelegas

The McCune Albright syndrome is seldom encountered and rarely reported in dental literature. It represents a special category of polyostic fibrous displasia associated with skin pigmentation and endocrine disturbances. We describe the case of a 9-year-old boy with the McCune Albright syndrome, who was treated for a mandibular osteolytic lesion.

Journal: :AVERROUS: Jurnal Kedokteran dan Kesehatan Malikussaleh 2019

Journal: :avicenna journal of dental research 0
masoumeh khoshhal department of periodontics, hamadan university of medical sciences, hamadan, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) nazli rabienejad department of periodontics, hamadan university of medical sciences, hamadan, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) abbas shokri department of radiology, hamadan university of medical sciences, hamadan, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) ali heidari department of oral and maxillofacial surgery, hamadan university of medical sciences, hamadan, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences) fariborz vafaee dental research center, department of prosthodontics, hamadan university of medical sciences, hamadan, ir iran; dental research center, department of prosthodontics, hamadan university of medical sciences, hamadan, ir iran. tel/fax: +98-8138241961سازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences)

discussion in this patient we preferred following up. afterwards, total surgical lesion resection can be performed. after a long-term follow-up, the area may receive an implant. case presentation a 40-year-old female patient presented an opaque lesion at the left mandibular side of face, in a cone-beam computerized tomography (cbct) view, during the implant placement evaluations. the patient ha...

2015
Claudia E Dumitrescu Michael T Collins

McCune-Albright syndrome (MAS) is classically defined by the clinical triad of fibrous dysplasia of bone (FD), café-au-lait skin spots, and precocious puberty (PP). It is a rare disease with estimated prevalence between 1/100,000 and 1/1,000,000. FD can involve a single or multiple skeletal sites and presents with a limp and/or pain, and, occasionally, a pathologic fracture. Scoliosis is common...

Journal: :Orphanet Journal of Rare Diseases 2008
Claudia E Dumitrescu Michael T Collins

McCune-Albright syndrome (MAS) is classically defined by the clinical triad of fibrous dysplasia of bone (FD), café-au-lait skin spots, and precocious puberty (PP). It is a rare disease with estimated prevalence between 1/100,000 and 1/1,000,000. FD can involve a single or multiple skeletal sites and presents with a limp and/or pain, and, occasionally, a pathologic fracture. Scoliosis is common...

Moein Mobini Rahim Vakili, Saba Vakili,

McCune-Albright syndrome (MAS) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. The disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  We describe a girl patient with MAS having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. Clinical presentat...

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