Results 21 to 30 of about 2,769 (118)

Mazabraud Syndrome Associated with McCune-Albright Syndrome: A Case Report and Literature Review

Case Reports in Oncology, 2023
The Mazabraud syndrome is a rare form of bone fibrous dysplasia associated with intramuscular myxomas. The McCune-Albright syndrome is characterized by the association of dysplasia fibrous bone to one or more extra-osseous manifestations, including café ...
Laurys Boudin, Valeria De Luca, Léna Mescam-Mancini, Vincent Niziers, Delphine Perrot, Jerome Guiramand, Audrey Monneur, Christophe Chagnaud, François Bertucci   +8 more
doaj   +1 more source

Scoliosis with peculiar radiological features in a patient with McCune‐Albright syndrome

Clinical Case Reports, 2021
Patients with McCune‐Albright Syndrome (MAS) should always attend regular follow‐up. Beside the endocrinological aspects, the screening must take into account osteoarticular complications such as scoliosis, even in patients without fibrous dysplasia.
Alexandre Michev, Luca Lungarotti, Maria Sole Prevedoni Gorone, Antonia Apicella, Giulia Di Vincenzo, Gian Luigi Marseglia, Ilaria Brambilla   +6 more
doaj   +1 more source

Hyperthyroidism related to McCune-Albright syndrome: report of two cases and review of the literature [PDF]

, 2008
INTRODUCTION: McCune-Albright syndrome is a sporadic disease clinicaly characterized by polyostotic fibrous dysplasia, café-au-lait cutaneous spots and hyperfunctional endocrinopathies, such as precocious puberty, hyperthyroidism, acromegaly and others ...
Abs R, Albin J, Albright F, Ana Carolina R. Sallum, Andrews SB, Benedict P, Brogan P, Cavanah SFW, Cohen MM Jr, de Sanctis C, Domenech E, D’Armiento M, Fernando D. Leonhardt, Feuillan PP, Feuillan PP, Firat D, Gallacher SJ, Giovanelli G, Halvorsen S, Hamilton CR Jr, Huang TS, Isotani H, Jervis GA, Kim JP, Lair-Milan F, Lawless ST, Lee PA, Leet AI, Mastorakos G, Mastorakos G, Mauras N, McCune DJ, Misaki M, Moldawer M, Márcio Abrahão, Onivaldo Cervantes, Peck FB, Reinaldo K. Yazaki, Richton SM, Riminucci M, Samuel S, Schwindinger WF, Shenker A, Shenker A, Sternberg WH, Summerfeldt P, Tanaka T, Vague J, Weinstein LS, Yettra M, Yoshimoto M, Zangeneh F   +51 more
core   +3 more sources

Delayed Diagnosis of McCune–Albright Syndrome

Case Reports in Genetics, 2021
Background. McCune–Albright syndrome (MAS) is a rare heterogeneous genetic disorder that is characterized by a triad of polyostotic fibrous dysplasia (FD), café au lait spots (CAL), and multiple hyperfunctional endocrinopathies.
Bereket Fantahun, Seblewongel Desta
doaj   +1 more source

Clinical, microscopic and imaging findings associated to Mccune-Albright syndrome: report of two cases [PDF]

, 2008
McCune-Albright syndrome is characterized by the triad café-au-lait cutaneous spots, polyostotic fibrous dysplasia and endocrinopathies. This article presents two cases of McCune-Albright syndrome in a middle-aged woman and a young girl.
BRENTEGANI, Luiz Guilherme, LACERDA, Suzie Aparecida, RIBEIRO, Michel Campos, SICCHIERI, Luciana Gonçalves, XAVIER, Samuel Porfírio   +4 more
core   +1 more source

Occurrence of testicular microlithiasis in androgen insensitive hypogonadal mice [PDF]

, 2009
<b>Background</b>: Testicular microliths are calcifications found within the seminiferous tubules. In humans, testicular microlithiasis (TM) has an unknown etiology but may be significantly associated with testicular germ cell tumors ...
AC Peterson, Ana Monteiro, BM Cattanach, C Lecureuil, CE Hoei-Hansen, DL Lam, Guido Verhoeven, HH Rashid, J Coffey, J Lang, K De Gendt, K Thomas, Karl De Gendt, L Murphy, LA Korde, M Nistal, M Nistal, M Vegni-Talluri, M Wasniewska, Margaret H Abel, NJ van Casteren, Peter J O'Shaughnessy, R Drut, RA Rey, S Zastrow   +24 more
core   +2 more sources

Cushing syndrome as a failed cardiac screen in a patient with McCune–Albright syndrome: a case report

Journal of Medical Case Reports, 2022
Background McCune–Albright syndrome is a complex disorder encompassing multiple endocrinopathies. These manifestations are secondary to a mutation in the stimulatory G-protein alpha subunit. Cushing syndrome is due to autonomous secretory function of the
Christy Foster, Hiba Al Zubeidi, Alicia Diaz-Thomas   +2 more
doaj   +1 more source

Atualização em etiologia, diagnóstico e manejo da precocidade sexual [PDF]

, 2008
Precocious puberty is defined as the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys. Gonadotropin-dependent precocious puberty (GDPP) results from the premature activation of the hypothalamic ...
ARNHOLD, Ivo J. P., BRITO, Vinicius Nahime, LATRONICO, Ana Claudia, MENDONÇA, Berenice Bilharinho   +3 more
core   +2 more sources

Gynecologic and reproductive outcomes in fibrous dysplasia/McCune-Albright syndrome

Orphanet Journal of Rare Diseases, 2019
Background Autonomous ovarian activation with recurrent estrogen-producing cysts is a hallmark feature of the rare bone and endocrine disorder fibrous dysplasia/McCune-Albright syndrome.
Alison M. Boyce, Rachel K. Casey, Diana Ovejero Crespo, Cynthia M. Murdock, Andrea Estrada, Lori C. Guthrie, Beth A. Brillante, Veronica Gomez-Lobo, Lynette K. Nieman, Michael T. Collins   +9 more
doaj   +1 more source

Optic disc Edema in patients with fibrous dysplasia/McCune-Albright syndrome: Craniomorphometric analysis and peripapillary retinal nerve fiber layer data

Data in Brief, 2021
This article reports quantitative measurements of intracranial volume, optic canal area, and peripapillary retinal nerve fiber layer (RNFL) for a cohort of 124 patients with craniofacial fibrous dysplasia/McCune-Albright Syndrome (FD/MAS), previously ...
Layne N. Raborn, Kristen S. Pan, Edmond J. FitzGibbon, Michael T. Collins, Alison M. Boyce   +4 more
doaj   +1 more source