Fibro-osseous lesion of maxilla. Report of two cases in a family with review of literature [PDF]
Fibrous dysplasia is a disturbance of bone metabolism that is classified as a benign fibro-osseous lesion. Fibrous connective tissue containing abnormal bone, replaces normal bone. The etiology of fibrous dysplasia is unknown.
Kaur, Bhawandeep +2 more
core +1 more source
The Role of gsp Mutations on the Development of Adrenal Cortical Tumors and Adrenal Hyperplasias
Somatic GNAS point mutations, commonly known as gsp mutations, are involved in the pathogenesis of McCune Albright syndrome and have also been described in autonomous hormone-producing tumors, such as somatotropinoma, corticotrophoma, thyroid cancer ...
Maria Candida Barisson Villares Fragoso +3 more
doaj +1 more source
Oral Alendronate Treatment for Severe Polyostotic Fibrous Dysplasia due to McCune-Albright Syndrome in a Child: A Case Report [PDF]
Polyostotic fibrous dysplasia (FD) associated to McCune-Albright Syndrome (MAS) often leads to fractures, deformities, and bone pain resulting in bad quality of life.
Aragão, Ana Luiza Andrade +1 more
core +3 more sources
EFFICACY OF HOMOGENOUS BONE GRAFTING IN MCCUNE-ALBRIGHT SYNDROME [PDF]
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 +4 more
core
Fibrous dysplasia of maxilla: Report of two cases
Fibrous dysplasia (FD) is an idiopathic skeletal disorder in which the trabecular bone is replaced and distorted by poorly organized, structurally unsound fibro-osseous tissue. The lesion is classified into two forms: Monostotic (75-80%) and polyostotic.
Nisha Dua +3 more
doaj +1 more source
Myelofibrosis and T3-thyreotoxicosis in a girl with McCune-Albright Syndrome [PDF]
Birgit Peitersen +3 more
openalex +1 more source
MECHANISM OF PRECOCIOUS PUBERTY IN GIRLS WITH McCUNE-ALBRIGHT SYNDROME (MAS) [PDF]
Carol M. Foster +6 more
openalex +1 more source
Resistência ao hormônio tireoidiano detectada por meio da triagem neonatal [PDF]
We report the clinical and laboratory findings, and molecular analysis of a Brazilian patient with resistance to thyroid hormone syndrome (RTH) detected by neonatal screening. The index case was born at term by normal delivery with 2,920 g and 45 cm. TSH
MACIEL, Léa Maria Zanini +1 more
core +1 more source
Activating Mutations of the Stimulatory G Protein in the McCune–Albright Syndrome [PDF]
Lee S. Weinstein +5 more
openalex +1 more source
Se presenta a un paciente de sexo femenino de 27 años de edad con el cuadro clásico de Síndrome de Mc Cune- Albright, caracterizado por: pubertad precoz, manchas color café con leche, displasia fibrosa poliostótica y gigantismo.
Javier Garcés +3 more
doaj

