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About 1,459 results

ALLMedicine™ Osteopetrosis Center

Research & Reviews  723 results

Transcriptomic and bioinformatic analysis of Clcn7-dependent Autosomal Dominant Osteope...
https://doi.org/10.1016/j.bone.2020.115828
Bone Norwood I, Szondi D et. al.

Dec 28th, 2020 - Autosomal Dominant Osteopetrosis type 2 (ADO2) is a rare genetic disease characterized by dense yet fragile bones. To date, the radiological approach remains the gold standard for ADO2 diagnosis. However, recent observations unveiled that ADO2 is ...

Paediatric bilateral femoral neck fractures in osteopetrosis treated conservatively.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737079
BMJ Case Reports; Kumar S, Dhammi IK et. al.

Dec 15th, 2020 - The treatment of pathological femoral neck fracture in children due to osteopetrosis is not clear as only a few cases have been reported to date. We encountered a 7-year-old osteopetrotic girl with asynchronous bilateral femoral neck fractures. Ra...

How we approach malignant infantile osteopetrosis.
https://doi.org/10.1002/pbc.28841
Pediatric Blood & Cancer; Even-Or E, Stepensky P

Dec 14th, 2020 - Malignant infantile osteopetrosis (MIOP) is a rare hereditary disorder characterized by excessive bone overgrowth due to a defect in bone marrow resorption by osteoclasts. In most cases, hematopoietic stem cell transplantation (HSCT) may correct b...

Minimally invasive cardiac surgery in a patient with osteopetrosis and symptomatic mitr...
https://doi.org/10.1111/jocs.15153
Journal of Cardiac Surgery; Kono T, Takagi K et. al.

Dec 7th, 2020 - Osteopetrosis is a rare hereditary bone development disorder caused by osteoclast dysfunction, which increases bone density. Although few studies have investigated cardiovascular disease in osteopetrosis, sternotomy outcomes in this condition are ...

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Drugs  2 results see all →

Clinicaltrials.gov  731 results

Transcriptomic and bioinformatic analysis of Clcn7-dependent Autosomal Dominant Osteope...
https://doi.org/10.1016/j.bone.2020.115828
Bone Norwood I, Szondi D et. al.

Dec 28th, 2020 - Autosomal Dominant Osteopetrosis type 2 (ADO2) is a rare genetic disease characterized by dense yet fragile bones. To date, the radiological approach remains the gold standard for ADO2 diagnosis. However, recent observations unveiled that ADO2 is ...

Paediatric bilateral femoral neck fractures in osteopetrosis treated conservatively.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737079
BMJ Case Reports; Kumar S, Dhammi IK et. al.

Dec 15th, 2020 - The treatment of pathological femoral neck fracture in children due to osteopetrosis is not clear as only a few cases have been reported to date. We encountered a 7-year-old osteopetrotic girl with asynchronous bilateral femoral neck fractures. Ra...

How we approach malignant infantile osteopetrosis.
https://doi.org/10.1002/pbc.28841
Pediatric Blood & Cancer; Even-Or E, Stepensky P

Dec 14th, 2020 - Malignant infantile osteopetrosis (MIOP) is a rare hereditary disorder characterized by excessive bone overgrowth due to a defect in bone marrow resorption by osteoclasts. In most cases, hematopoietic stem cell transplantation (HSCT) may correct b...

Minimally invasive cardiac surgery in a patient with osteopetrosis and symptomatic mitr...
https://doi.org/10.1111/jocs.15153
Journal of Cardiac Surgery; Kono T, Takagi K et. al.

Dec 7th, 2020 - Osteopetrosis is a rare hereditary bone development disorder caused by osteoclast dysfunction, which increases bone density. Although few studies have investigated cardiovascular disease in osteopetrosis, sternotomy outcomes in this condition are ...

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News  3 results

A 49-Year-Old Man With Pain at the Site of a Previous Fracture
https://reference.medscape.com/viewarticle/857143_5

Jan 13th, 2016 - On initial presentation, exclusion of other diseases that result in a similar "bright bone" appearance on radiography is important. The causes of diffuse osteosclerosis include hypervitaminosis D, hypoparathyroidism, myelofibrosis, Paget disease, ...

HLA-matched sibling transplants provide best outcomes in infantile osteopetrosis
https://www.mdedge.com/rheumatology/article/101309/transfusion-medicine/hla-matched-sibling-transplants-provide-best
Lucas Franki

Jul 18th, 2015 - Long-term survival after hematopoietic stem cell transplantation for infantile osteopetrosis was highest when grafts were taken from human leukocyte antigen (HLA)-matched siblings, according to the largest cohort of patients with the disease that.

Pyle-type Metaphyseal Dysplasia
https://www.medscape.com/viewarticle/709818_3

Diagnosis Pyle-type metaphyseal dysplasia (or Pyle's disease) Differential diagnosis: Chronic anemia (e.g. Sickle-cell disease), osteopetrosis, Gaucher disease and Niemann-Pick disease.

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