نتایج جستجو برای: maccune albright syndrome

تعداد نتایج: 622258  

Journal: :Journal of radiology case reports 2010
Justin Clark William Carson

We present the case of a patient with craniofacial polyostotic fibrous dysplasia. Polyostotic fibrous dysplasia is relatively rare and usually presents in late childhood/early adulthood. It is occasionally associated with endocrine disorders such as McCune-Albright syndrome. The benign pathology of this bone tumor belies its implications in the region of the skull base. Craniofacial polyostotic...

2016
Hao Shen Sudeep B Shrestha Xiang Fang Hao Liu Jun Lin Huilin Yang

A 26-year-old female patient suffered from intermittent back pain for 4 years and a fall from bicycle aggravated the symptom. Physical and imaging examinations revealed the diagnosis of polyostotic fibrous dysplasia in McCune-Albright syndrome. No neurological symptom was found. A vertebral fracture was seen at the eighth thoracic body. Percutaneous kyphoplasty was performed at the fractured le...

2011
Zehra Aycan Aşan Önder Semra Çetinkaya

McCune-Albright syndrome (MAS) is characterized by the triad of fibrous dysplasia (FD), cafe-au-lait spots and precocious puberty (PP). We report a 14-year-old girl with MAS who has been followed-up for 8 years. She was referred for multiple fractures and vaginal bleeding at age 5.9 years. She had peripheral PP, FD, and osteoporosis and was diagnosed as MAS. The patient was treated with aromata...

2012
Eun Ju Son Vânia Nosé

Follicular cell-derived well-differentiated thyroid cancer, papillary (PTC) and follicular thyroid carcinomas comprise 95% of all thyroid malignancies. Familial follicular cell-derived well-differentiated thyroid cancers contribute 5% of cases. Such familial follicular cell-derived carcinomas or non-medullary thyroid carcinomas (NMTC) are divided into two clinical-pathological groups. The syndr...

Journal: :American journal of medical genetics. Part A 2013
Sérgio B Sousa Margarida Venâncio Estelle Chanudet Rodger Palmer Lina Ramos Philip L Beales Gudrun E Moore Jorge M Saraiva Raoul C Hennekam

Here we report on a Portuguese family with three sisters who shared moderate intellectual disability, unusual facial morphology (short palpebral fissures; broad nasal tip; thin upper and lower vermillion; broad and pointed chin) and hand anomalies in two of them (short left third and fifth right metacarpals in one case; marked syndactyly between the third and fourth fingers in another). One of ...

Journal: :Endocrine Abstracts 2016

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