Results 81 to 90 of about 12,028 (243)

Legius syndrome: Case report and review of literature [PDF]

, 2015
A 8-month-old child was referred to our Dermatologic Unit for suspected Neurofibromatosis type 1 (NF 1), because of the appearance, since few days after birth, of numerous caf\ue9-au-lait spots (seven larger than 5 mm); no other sign evocative of NF 1 ...
Belcaro, Chiara, Benelli, Elisa, Berti, Irene, Bruno, Irene, Ventura, Alessandro   +4 more
core   +2 more sources

Escondido pelo cabelo - um caso de puberdade precoce [PDF]

, 2020
McCune-Albright syndrome (MAS) is one of the conditions causing precocious gonadotropin-independent puberty. It is a rare disease, characterized by two of the three following features: precocious puberty, polyostotic fibrous dysplasia (PFD), and café au ...
Costa, Sara T., Ferreira, Filipa A., Pereira, Carla, Robalo, Brígida, Sampaio, Lurdes   +4 more
core   +1 more source

Late‐Onset Nonhereditary Cherubism: First Reported Case in Ghana With Review of Diagnostic and Management Challenges

Case Reports in Radiology, Volume 2025, Issue 1, 2025.
Background Cherubism is a rare genetic disorder characterised by multilocular cystic lesions in the mandible and/or maxilla, which result in the typical cherub‐like face. Two forms of cherubism exist—hereditary (familial) and nonhereditary (nonfamilial)—and it usually occurs amongst children aged 2–7 years.
Seth Kwadjo Angmorterh, Mariella Mawunyo Amoussou-Gohoungo, Adam Inusah, Bridgette Palm, Kafui Kossi Kekessie, Riaan van de Venter, Sonia Aboagye, Cosmos Yarfi, John Nsor-Atindana, Portia Mamle Angmorterh, Klenam Dzefi-Tettey, Anusha Vaddi   +11 more
wiley   +1 more source

Effect of intranasal calcitonin in a patient with McCune-Albright Syndrome, fibrous dysplasia, and refractory bone pain [PDF]

, 2017
McCune-Albright syndrome (MAS) is a rare disease defined by the triad of polyostotic fibrous dysplasia of bone, caf´e-au-lait skin spots, and precocious puberty. No available treatment is effective in changing the course of fibrous dysplasia of bone, but
Fighera, Tayane Muniz, Spritzer, Poli Mara   +1 more
core   +5 more sources

Recovery of neurological deficit after posterior total en-bloc resection of locally aggressive polyostotic fibrous dysplasia

Journal of Orthopaedic Reports
Summary of background data: A case report of polyostotic and locally aggressive fibrous dysplasia including thoracic spine and rib with the symptom of neurologic deficit. In adulthood Polyostotic fibrous dysplasia which occurs in mature bone and behavior
Abdullah Iyigun, Omer Polat, Bekir Yavuz Ucar, Necdet Saglam   +3 more
doaj   +1 more source

A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding [PDF]

, 2011
Background: McCune-Albright syndrome (MAS) is a rare non-inherited disorder characterized by the clinical triad of precocious puberty, cafe-au-lait skin lesions, and fibrous dysplasia of bone.
Hashemipour, M., Hekmatnia, A., Hovsepian, S., Kelishadi, R., Rostampour, N.   +4 more
core   +1 more source

Lower limb lengthening and deformity correction in polyostotic fibrous dysplasia using external fixation and flexible intramedullary nailing.

Journal of Orthopaedics, 2020
The study describes preliminary experience of the use of external fixators for limb lengthening and deformity correction in combination with flexible intramedullary nailing in management of polyostotic fibrous dysplasia.
A. Popkov, A. Aranovich, A. Antonov, P. Journeau, P. Lascombes, D. Popkov   +5 more
semanticscholar   +1 more source

RANK‐L inhibitor as a promising agent for refractory extensive craniofacial fibrous dysplasia: A case report

Head &Neck, Volume 46, Issue 1, Page E1-E5, January 2024.
Abstract Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of permanent visual impairment.
Moataz D. Abouammo, Mohammad Bilal Alsavaf, Daniel M. Prevedello, Luma Ghalib, Alison M. Boyce, Ricardo L. Carrau   +5 more
wiley   +1 more source

Fibrous Dysplasia: Clinicopathologic Presentation of 36 Cases

Türk Patoloji Dergisi, 2018
Objective: Fibrous dysplasia is a slowly progressing bone lesion resulting from displacement of the normal medullary bone with abnormal fibroosseous tissue.
Mine ÖZŞEN, Ülviye YALÇINKAYA, Muhammed Sadık BILGEN, Zeynep YAZICI   +3 more
doaj   +1 more source

A narrative review of the literature on the pediatric orthopedic management of fibrous dysplasia. [PDF]

Front Pediatr
Fibrous dysplasia is a congenital, non-inherited, benign intramedullary bone lesion in which the normal bone marrow is replaced by abnormal fibro-osseous tissue.
Paris E, De Marco G, Vazquez O, Steiger C, Boudabbous S, Dayer R, Ceroni D.   +6 more
europepmc   +2 more sources