Results 71 to 80 of about 10,613 (196)

Benign osteopetrosis with secondary osteomyelitic changes in the mandible: A report of two rare cases

Journal of Indian Academy of Oral Medicine and Radiology, 2009
Osteopetrosis is a name given to a group of diseases that affect the growth and remodeling of the bone. It is characterized by overgrowth and sclerosis of bone, with a resultant thickening of bony cortices and narrowing of marrow cavities throughout the ...
S Jayachandran, S.S.A Mohamed Riyaz, L Kayal   +2 more
doaj   +1 more source

Proximal femoral fracture surgery in a patient with osteopetrosis tarda: complications and treatment strategy

, 2016
Fırat Seyfettinoglu, Ümit Tuhanioğlu, Hasan Ulas Ogur, Hakan Cicek Department of Trauma and Orthopedics, Adana Numune Training and Educational Hospital, Adana, Turkey Abstract: Osteopetrosis is a rare, inherited disease ...
Tuhanioglu U, Cicek H, Ogur HU, Seyfettinoglu F   +3 more
core  

Neurosurgical aspects of marble bone disease: treatment modalities and outcome

Egyptian Journal of Neurosurgery
Background Marble bone disease or osteopetrosis is an extremely rare hereditary condition that causes abnormal bone density and fragility due to impaired osteoclastic action.
Mahmoud Mohammed Gamal, Roshdy Elkhayat, Hassan Mohammed Hassan   +2 more
doaj   +1 more source

Osteopetrosis as a rare cause of anaemia in paediatric patients: a case report

Pediatria i Medycyna Rodzinna, 2019
Anaemia is a common manifestation in paediatric patients. The most common cause of anaemia is iron deficiency. In differential diagnosis not only the most common diseases resulting in haemoglobin decrease should be considered, but also those less common.
Anna Fałkowska, Janina Marta Choma, Dominik Grabowski, Katarzyna Drabko   +3 more
doaj   +1 more source

Society for Maternal‐Fetal Medicine Consult Series #75: Evaluation and management of non‐immune hydrops fetalis

Pregnancy, Volume 2, Issue 2, March 2026.
Abstract Non‐immune hydrops fetalis (NIHF) can result from a multitude of underlying causes, such as fetal genetic diseases, congenital anomalies, infections, fetal arrhythmias, placental tumors, monochorionic twin complications, and other disorders.
Society for Maternal‐Fetal Medicine (SMFM), Teresa. N. Sparks, Mary. E. Norton, SMFM Publications Committee   +3 more
wiley   +1 more source

Osteopetrosis: Reporte de un caso [PDF]

, 2013
La osteopetrosis o enfermedad de Albers Schönberg, pertenece al grupo de las osteocondrodisplasias.Es una rara enfermedad ósea hereditaria donde observamos la falla en la resorción y modelación ósea por defecto en la función de los osteoclastos.La ...
Maldonado Martínez, Mercy Dolores, Acosta Vera, Silvia Anabela   +1 more
core  

Infantile osteopetrosis with superimposed rickets

, 2013
Rickets is a complication of infantile osteopetrosis and pre-treatment recognition of this complication is important. To describe four children with infantile osteopetrosis complicated by rickets (osteopetrorickets) and review the relevant literature.

core   +1 more source

3D Multicellular Scaffold Based Model for Advancing Bone Disorder Research

Advanced Functional Materials, Volume 36, Issue 13, 12 February 2026.
A scalable 3D multicellular in vitro bone model engineered by integrating osteoblasts, osteoclasts, and endothelial cells on biodegradable scaffolds. The system recapitulates key features of human bone remodeling and disease pathology. As a proof of concept, the model mimics osteogenesis imperfecta, demonstrating its potential as a physiologically ...
Gali Guterman‐Ram, Majd Machour, Janette Zavin, Roy Meretzki, Reut Lev‐Ari, Shulamit Levenberg   +5 more
wiley   +1 more source

Case report: A 10 years follow-up of periprosthetic femoral fracture after total hip arthroplasty in osteopetrosis

Chinese Journal of Traumatology, 2017
Osteopetrosis is an inherited disorder characterized by increased bone density and brittle bone quality. Degenerative changes often occur after the age of 40 in patients with osteopetrosis.
Zhan-Feng Zhang, Dan Wang, Li-Dong Wu, Xue-Song Dai   +3 more
doaj   +1 more source

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

BMC Medical Genetics, 2017
Background Osteopetrosis is a rare inherited bone disorder mainly described as an increased bone density caused by defective osteoclastic bone resorption. To date, genetic variants of eleven genes have been reported so far to be associated with different
Muhammad Ajmal, Asif Mir, Sughra Wahid, Chiea Chuen Khor, Jia Nee Foo, Saima Siddiqi, Mehran Kauser, Salman Akbar Malik, Muhammad Nasir   +8 more
doaj   +1 more source