Results 41 to 50 of about 2,181,916 (247)
McCune-Albright Syndrome: A-rare-case report [PDF]
, 2022 McCune-Albright syndrome (MAS) is a rare genetic disordered originally recognized by the triad of polyostotic fibrous dysplasia, precocious puberty, and cafe-au-late spots. We report a case of 2 years-11-month-old girl who came with complaints ...
Angriani, Hadia +3 more
core +2 more sources
Journal of Cosmetic Dermatology, Volume 22, Issue 12, Page 3213-3222, December 2023., 2023 Abstract Background Reflectance confocal microscopy (RCM) has quickly transitioned from a research tool to an adjunct diagnostic bedside tool, providing the opportunity for noninvasive evaluation of skin lesions with histologic resolution. RCM is an optical imaging technique that uses near‐infrared excitation wavelengths and safe low‐power lasers.
Banu Farabi +5 more
wiley +1 more source
Phenotyping Pain in Patients With Fibrous Dysplasia/McCune-Albright Syndrome.
J Clin Endocrinol Metab, 2023 CONTEXT Pain is a poorly managed aspect in fibrous dysplasia/McCune-Albright Syndrome (FD/MAS) due to uncertainties regarding the clinical, behavioral, and neurobiological underpinnings that contribute to pain in these patients.
Golden E +12 more
europepmc +2 more sources
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 +6 more
doaj +1 more source
Fibrous dysplasia/McCune-Albright syndrome: a rare, mosaic disease of Gαs activation.
Endocrine reviews, 2019 Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare disorder of striking complexity. It arises from somatic, gain-of-function mutations in GNAS, leading to mosaic Gαs activation and inappropriate production of intracellular cyclic adenosine ...
A. Boyce, M. Collins
semanticscholar +1 more source
A rare case of McCune Albright syndrome [PDF]
, 2019 McCune Albright syndrome is characterized by the clinical triad of precocious puberty, polyostotic fibrous dysplasia, and café-au-lait pigmentation. Authors reported the case of a 6 years old girl presenting with vaginal bleeding.
Banga, Siftie-Kaur, Patil, Pooja
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 +9 more
doaj +1 more source
Adaptive syndrome measurements for Shor-style error correction [PDF]
Quantum 7, 1075 (2023), 2022 The Shor fault-tolerant error correction (FTEC) scheme uses transversal gates and ancilla qubits prepared in the cat state in syndrome extraction circuits to prevent propagation of errors caused by gate faults. For a stabilizer code of distance $d$ that can correct up to $t=\lfloor(d-1)/2\rfloor$ errors, the traditional Shor scheme handles ancilla ...
arxiv +1 more source
Treatment of Girls and Boys with McCune-Albright Syndrome with Precocious Puberty - Update 2017 [PDF]
, 2017 The most common endocrinopathy associated with McCune-Albright Syndrome (MAS) is peripheral precocious puberty (PP) which occurs far more often in girls than in boys.
Eugster, Erica A., Neyman, Anna
core +1 more source
Syndrome decoding by quantum approximate optimization [PDF]
Quantum Inf Process 23, 368 (2024), 2022 The syndrome decoding problem is known to be NP-complete. The goal of the decoder is to find an error of low weight that corresponds to a given syndrome obtained from a parity-check matrix. We use the quantum approximate optimization algorithm (QAOA) to address the syndrome decoding problem with elegantly-designed reward Hamiltonians based on both ...
arxiv +1 more source