Results 81 to 90 of about 2,769 (118)

Fertility journey of a patient with McCune-Albright syndrome associated with bilateral ovarian involvement

F&S Reports
Objective: To report a patient with McCune-Albright syndrome (MAS) with bilateral ovarian involvement who had achieved a pregnancy through in vitro fertilization (IVF). Design: Case report. Setting: Academic fertility center.
Joanna J. Kim, M.D., Stephanie Dufour, M.D., Sara Awad, M.B.B.S., M.H.P.E., Bryden Magee, M.D.   +3 more
doaj   +1 more source

Genetic diseases of renal phosphate handling [PDF]

, 2017
UNLABELLED: Renal control of systemic phosphate homeostasis is critical as evident from inborn and acquired diseases causing renal phosphate wasting. At least three transport proteins are responsible for renal phosphate reabsorption: NAPI-IIa (SLC34A1 ...
Biber, Jürg, Hernando, Nati, Rubio-Aliaga, Isabel, Wagner, Carsten A.   +3 more
core   +3 more sources

McCune-Albright Syndrome with Hypophosphatemic Rickets

Journal of the ASEAN Federation of Endocrine Societies, 2015
Fibrous dysplasia (FD) is sometimes accompanied by extraskeletal manifestations that can include any combination of café-au-lait macules, hyperfunctioning endocrinopathies, such as gonadotropin-independent precocious puberty, hyperthyroidism, growth ...
Manish Gutch, Sukriti Kumar, Keshav Kumar Gupta, Abhinav Kumar Gupta, Syed Mohd Razi   +4 more
doaj  

A rare case of solitary toxic nodule in a 3yr old female child – a case report [PDF]

, 2013
A three year old hyperactive female child presented with a midline neck swelling of one year duration. Clinical examination revealed a nodule in the isthmus of thyroid.Her Thyroid Stimulating Hormone (TSH) was suppressed and Free T3 and Free T4 levels ...
Karunakaran, Poongkodi, Maharajan, Chandrasekaran   +1 more
core   +1 more source

Severe Neonatal Cholestasis as an Early Presentation of McCune- Albright Syndrome

JCRPE, 2019
McCune-Albright syndrome (MAS) is a rare genetic disorder characterized by café-au-lait macules, polyostotic fibrous dysplasia and multiple endocrinopathies. Liver involvement, although described, is a rare complication.
Nicole Coles, Ian Comeau, Tatiana Munoz, Jennifer Harrington, Roberto Mendoza-Londono, Andreas Schulze, Sari Kives, Binita M. Kamath, Jill Hamilton   +8 more
doaj   +1 more source

EFFICACY OF HOMOGENOUS BONE GRAFTING IN MCCUNE-ALBRIGHT SYNDROME [PDF]

, 1985
A case of McCune-Albright syndrome is reported. The patient was a girl aged 8 years. The chief complaints were gait disturbance and a limp. Roentgenograms showed collapse and severe varus deformity of the femoral neck on the right side with 64° of neck ...
FUJITA, Atsushi, IKEDA, Toshihiko, KASAHARA, Katsuyuki, OKUMURA, Hideo, YAMAMURO, Takao   +4 more
core  

McCune-Albright syndrome case report [PDF]

Introduction: McCune Albright syndrome (SMA) is considered a rare genetic disease, characterized by bone dysplasia, endocrine disorders and hyperpigmentary skin lesions.
Cabrera Pacheco, Reinaldo, Cordero Betancourt, Lázaro Leduan, Díaz Domínguez, Rafael, Mesa Martí, Mario, Reyes Chirino, Guillermo   +4 more
core   +2 more sources

McCune Albright Syndrome (MAS) : polyostotic fibrous dysplasia [PDF]

, 2017
Augsburg, Lukasz, Gielen, Jan, Vanhoenacker, Filip   +2 more
core   +2 more sources

گزارش يک مورد سندرم آلبرايت [PDF]

, 2004
سندرم آلبرايت (Mccune –Albright) بيماری است که با فيبروز ديسپلازی منتشر، بلوغ جنسی زودرس و پيگمانتاسيون پوست تظاهر می‌کند. يافته‌های بالينی عبارتند از: پيگمانتاسيون پوست(Café-au-lait) که در ابتدای تولد ظاهر می‌شود.
فتحی, تیمور, فراهينی, حسین   +1 more
core  

Management of pediatric testicular microlithiasis

Frontiers in Pediatrics
Testicular microlithiasis (TM) is a primarily asymptomatic condition characterized by the accumulation of microscopic calcium deposits within the seminiferous tubules.
Hunter A. Flores, Hunter A. Flores, Walker C. Bailey, Walker C. Bailey, Kelly T. Harris   +4 more
doaj   +1 more source