نتایج جستجو برای: mccune albright syndrome

تعداد نتایج: 622355  

2011
Cécile Nozières Pascale Berlier Clémentine Dupuis Catherine Raynaud-Ravni Yves Morel Françoise Borson Chazot Marc Nicolino

BACKGROUND Somatotropinoma, a pituitary adenoma characterised by excessive production of growth hormone (GH), is extremely rare in childhood. A genetic defect is evident in some cases; known genetic changes include: multiple endocrine neoplasia type 1 (MEN1); Carney complex; McCune-Albright syndrome; and, more recently identified, aryl hydrocarbon receptor-interacting protein (AIP). We describe...

2011
Sanjay Kumar Bhadada Anil Bhansali Sambit Das Ramanbir Singh R. Sen A. Agarwal B.R. Mittal Uma Nahar Pinaki Dutta Niranjan Khandelwal

BACKGROUND & OBJECTIVES Fibrous dysplasia (FD) is a rare metabolic bone disease and information available from India is limited to only anecdotal case reports. We describe the clinical profile and therapeutic outcome of 25 patients with FD observed over a period of 14 yr in a tertiary care centre from north India. METHODS In this retrospective study patients (n = 25) with diagnosis of fibrous...

2015
Tong Li Yak-Nam Wang Tatiana D. Khokhlova Samantha D’Andrea Frank Starr Hong Chen Jeannine S. McCune Linda J. Risler Afshin Mashadi-Hossein Joo Ha Hwang

Pulsed high intensity focused ultrasound (pHIFU) enhances delivery of doxorubicin in a preclinical model of pancreatic cancer Tong Li, Yak-Nam Wang, Tatiana D. Khokhlova, Samantha D’Andrea, Frank Starr, Hong Chen, Jeannine S. McCune, Linda J. Risler, Afshin Mashadi-Hossein, Joo Ha Hwang 1 Center for Industrial and Medical Ultrasound, Applied Physics Laboratory, University of Washington, Seattle...

Journal: :Indian journal of pediatrics 2006
Seema Kapoor Siddhartha Gogia Ritu Paul Sharmila Banerjee

Albright's hereditary osteodystrophy is a rare inherited metabolic disorder characterized by a typical phenotype. It may be associated with or without resistance to parathyroid hormone (pseudohypoparathyroidism). Both forms may co-exist in the same family. Pseudohypoparathyroidism Type 1 and Pseudo-pseudohypoparathyroidism occur as a consequence of reduced erythrocyte membrane coupled with Gs a...

2013
Surojit Mondal Aniket Chowdhury Goutam Bandyopadhyay

Fibrous Dysplasia of bone is an uncommon congenital skeletal disorder that is found equally in both genders and is not inherited. Fibrous Dysplasia is characterized either monostotic or polyostotic, and may occur as a component of McCune Albright Syndrome or the rare Mazabraud Syndrome. Long bones, skull bones and ribs are most commonly affected bones. We present a case of a 18 years old boy ha...

2014
TMU J. Dent Mansi Agarwal Geetanshu Dawar Neelakshi S Rallan

Fibrous dysplasia (FD) is a benign intramedullary fibroosseous lesion originally described by Lichtenstein in 1938 and by Lichtenstein and Jaffe in 1942. 1 This is a benign dysplastic process of altered osteogenesis that may occur within a single bone (monostotic) or multiple bones (polyostotic), 2 and is best understood as a dysplastic anomaly of bone forming mesenchymal tissue. 3 It is a spor...

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