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osteopetrosis - hardened bones
Definition for osteopetrosis
Osteopetrosis / marble bone disease, Albers-Schonberg disease / is an extremely rare inherited disorder whereby the bones harden, becoming denser.
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Osteopetrosis / marble bone disease, Albers-Schonberg disease / is an extremely rare inherited disorder whereby the bones harden, becoming denser.
Normally, bone growth is a balance between osteoblasts (cells that create bone tissue) and osteoclasts (cells that destroy bone tissue). Sufferers of osteopetrosis have a deficiency of osteoclasts, meaning too much bone is being created. Despite this excess bone formation, people with osteopetrosis tend to have bones that are more brittle than normal. Mild osteopetrosis may cause no symptoms, and present no problems. However, serious forms can result in stunted growth, deformity, increased likelihood of fractures, and anaemia. It can also result in blindness, facial paralysis, and deafness, due to the increased pressure put on the nerves by the extra bone.
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anemia
hearing loss
vision problems
washed out look
some related diagnoses
1 - 7 of
59
diagnoses
drugs and toxins
hypothyroidism
retinitis pigmentosa
Alport's Syndrome
systemic lupus erythematosis
Friedreich's ataxia
Turner's Syndrome
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do i have 'osteopetrosis'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'osteopetrosis'
1 - 5 of
12
diagnostic tests
Skeletal radiograph survey
osteopetrosis and Skeletal radiograph survey
Serum Creatine Phosphokinase isoform BB (CPK-BB)
osteopetrosis and Serum Creatine Phosphokinase isoform BB (CPK-BB)
Serum Parathyroid hormone (PTH)
osteopetrosis and Serum Parathyroid hormone (PTH)
Serum bone-specific alkaline phosphatase
osteopetrosis and Serum bone-specific alkaline phosphatase
Serum calcium
osteopetrosis and Serum calcium
Molecular Genetic Studies
osteopetrosis and Molecular Genetic Studies
Magnetic Resonance Imaging (MRI)
osteopetrosis and Magnetic Resonance Imaging (MRI)
CT external ear
osteopetrosis and CT external ear
CT middle ear
osteopetrosis and CT middle ear
CT scan
osteopetrosis and CT scan
Serum Prostatic acid phosphatase (PAP)
osteopetrosis and Serum Prostatic acid phosphatase (PAP)
Smear for acanthocytes
osteopetrosis and Smear for acanthocytes
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therapeutic procedures for 'osteopetrosis'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for osteopetrosis:
therapeutic procedure search results for 'osteopetrosis'
1 - 3 of
3
therapeutic procedures
rankings are computer generated. please consult your health care provider.
Orthopedic surgical care
osteopetrosis and Orthopedic surgical care
Bone Marrow Transplant
osteopetrosis and Bone Marrow Transplant
Histocompatibility testing
osteopetrosis and Histocompatibility testing
medications search results for 'osteopetrosis'
1 - 4 of
4
medications
rankings are computer generated. please consult your health care provider.
Vitamin D
(a.k.a Vitamin D, calcitriol)
osteopetrosis and Vitamin D
Erythropoietin
osteopetrosis and Erythropoietin
Interferon gamma 1b
osteopetrosis and Interferon gamma 1b
Prednisone
osteopetrosis and Prednisone
web search results for osteopetrosis
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1 - 50
- osteopetrosis
Osteopetrosis - Wikipedia, the free encyclopedia
Osteopetrosis, literally "stone bone", also known as marble bone disease and ... International Osteopetrosis Association ... wikipedia.org/wiki/Osteopetrosis" ...
http://en.wikipedia.org/wiki/Osteopetrosis
en.wikipedia.org
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Osteopetrosis - Glossary Entry - Genetics Home Reference
congenital osteopetrosis. marble bone disease. osteosclerosis fragilis. Definition(s) A condition characterized by abnormal thickening and hardening of bone: as a: a ...
http://ghr.nlm.nih.gov/ghr/glossary/osteeopetrosis
ghr.nlm.nih.gov
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Osteopetrosis - Yahoo! Health
Important It is possible that the main title of the report Osteopetrosis is not the name you expected. Please check the synonyms listing to find the alternate name ...
http://health.yahoo.com/other-other/osteopetrosis/healthwise--nord354.html
health.yahoo.com
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CLCN7-Related Osteopetrosis
The spectrum of CLCN7-related osteopetrosis includes infantile ... autosomal dominant osteopetrosis type II (ADOII, Albers-Schoenberg disease) ...
http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...
www.ncbi.nlm.nih.gov
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Bisphosphonate-induced exposed bone (osteonecrosis/osteopetrosis) of ...
... induced exposed bone (osteonecrosis/osteopetrosis) of the jaws: risk factors, ... Osteopetrosis/chemically induced* Osteopetrosis/diagnosis. Osteopetrosis/therapy ...
http://www.ncbi.nlm.nih.gov/pubmed/16243172
www.ncbi.nlm.nih.gov
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Marble bone disease: a review of osteopetrosis and its oral health ...
Osteopetrosis is one cause of osteosclerosis and may result in such serious oral ... osteopetrosis and to provide guidance to dentists on the management of patients ...
http://www.ncbi.nlm.nih.gov/pubmed/18028760
www.ncbi.nlm.nih.gov
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Retroviruses, immunosuppression and osteopetrosis.
Retroviruses, immunosuppression and osteopetrosis. Labat ML. ... These similarities have prompted this review of retrovirus-induced osteopetrosis in animals. ...
http://www.ncbi.nlm.nih.gov/pubmed/3017470
www.ncbi.nlm.nih.gov
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Osteopetrosis cured by temporary parabiosis.
1: Science. 1973 May 25;180(88):875. Osteopetrosis cured by temporary parabiosis. ... The excessive accumulations of spongiosa in the long bones of congenitally ...
http://www.ncbi.nlm.nih.gov/pubmed/4706681
www.ncbi.nlm.nih.gov
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Osteopetrosis.
Osteopetrosis is a rare hereditary bone disorder that presents in one ... Osteopetrosis tarda is usually discovered accidentally on routine radiographs ...
http://www.ncbi.nlm.nih.gov/pubmed/9531912?dopt=Abstract
www.ncbi.nlm.nih.gov
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Osteopetrosis associated transmembrane protein 1, mRNA (cDNA clone MGC ...
Mouse protein-coding gene Ostm1. Represented by 137 ESTs from 86 cDNA libraries. ... Mus musculus osteopetrosis associated transmembrane protein 1, mRNA (cDNA clone ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=46636
www.ncbi.nlm.nih.gov
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Osteopetroses: Bone and Connective Tissue Disorders in Children: Merck ...
Osteopetrosis with delayed manifestations (Albers-Schönberg disease) ... This type of osteopetrosis is autosomal recessive, malignant, and congenital, ...
http://www.merck.com/mmpe/print/sec19/ch284/ch284m.html
www.merck.com
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Osteopetrosis associated transmembrane protein 1 (Ostm1)
Norway rat protein-coding gene Ostm1. Represented by 8 ESTs from 7 cDNA libraries. ... Rattus norvegicus osteopetrosis associated transmembrane protein 1, mRNA (cDNA ...
http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=163435
www.ncbi.nlm.nih.gov
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Localization of the gene causing autosomal dominant osteopetrosis type ...
... gene causing autosomal dominant osteopetrosis type I to chromosome 11q12 ... ADOI is the only type of osteopetrosis not associated with an increased fracture ...
http://www.ncbi.nlm.nih.gov/pubmed/12054167
www.ncbi.nlm.nih.gov
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Osteopetroses: Bone and Connective Tissue Disorders in Children: Merck ...
Osteopetrosis with delayed manifestations (Albers-Schönberg disease) ... Osteopetrosis with renal tubular acidosis: This type is autosomal recessive. ...
http://www.merck.com/mmpe/sec19/ch284/ch284m.html
www.merck.com
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summary
Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal ...
... recessive disorder that produces osteopetrosis, renal tubular acidosis, and ... exception, all patients with osteopetrosis and renal tubular acidosis examined ...
http://www.ncbi.nlm.nih.gov/pubmed/15300855
www.ncbi.nlm.nih.gov
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The deficiency of immunoregulatory receptor PD-1 causes mild osteopetrosis.
Nagahama K, Aoki K, Nonaka K, Saito H, Takahashi M, Varghese BJ, Shimokawa H, ... Osteopetrosis/blood. Osteopetrosis/genetics* Phenotype. Tibia/pathology. Substances: ...
http://www.ncbi.nlm.nih.gov/pubmed/15542030
www.ncbi.nlm.nih.gov
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Autosomal recessive osteopetrosis
Autosomal recessive "malignant" osteopetrosis is a rare congenital disorder of ... Osteopetrosis has been reported in most ethnic ...
http://www.orpha.net/data/patho/GB/uk-malosteo.pdf
www.orpha.net
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Carbonic anhydrase II deficiency syndrome: recessive osteopetrosis with ...
... recessive syndrome includes osteopetrosis with renal tubular acidosis ... Radiographic evidence of osteopetrosis was probably absent at birth but appeared ...
http://www.ncbi.nlm.nih.gov/pubmed/3081869
www.ncbi.nlm.nih.gov
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WebMD Health A-Z - Find reliable health and medical information on ...
Find a comprehensive index of trusted health and medical information. It is your ultimate guide to reliable health ... Osteopetrosis. Osteoporosis Center ...
http://www.webmd.com/a-to-z-guides/health-topics/op-ot.htm
www.webmd.com
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IKBKG - inhibitor of kappa light polypeptide gene enhancer in B-cells ...
... ectodermal dysplasia with immunodeficiency, osteopetrosis, and lymphedema. ... kinase ; lymphedema ; mutation ; mycobacterium ; nucleus ; osteopetrosis ; ...
http://ghr.nlm.nih.gov/gene=ikbkg
ghr.nlm.nih.gov
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Locus heterogeneity of autosomal dominant osteopetrosis (ADO).
White KE, Koller DL, Takacs I, Buckwalter KA, Foroud T, Econs MJ. ... Autosomal dominant osteopetrosis (ADO), is a heritable disorder that results ...
http://www.ncbi.nlm.nih.gov/pubmed/10084593
www.ncbi.nlm.nih.gov
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Osteopetroses: Bone Disorders: Merck Manual Home Edition
Osteopetrosis that occurs in infancy is fatal if not treated. ... In osteopetrosis (sometimes called marble bones), the body does not recycle old bone cells. ...
http://www.merck.com/mmhe/print/sec23/ch278/ch278j.html
www.merck.com
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Persistent viral DNA synthesis associated with an avian osteopetrosis ...
Persistent viral DNA synthesis associated with an avian osteopetrosis-inducing virus. ... play a significant role in the pathogenesis of MAV-2(O) osteopetrosis. ...
http://www.ncbi.nlm.nih.gov/pubmed/2548335?dopt=Abstract
www.ncbi.nlm.nih.gov
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Medical Terms - Explaining The Terminology - MedicineNet - Health and ...
Read doctor-produced health and medical information written for you to ... In osteoarthritis, osteopetrosis (stonelike bone), osteoporosis, etc. oto-: The ear. ...
http://www.medicinenet.com/script/main/art.asp?articlekey=6963
www.medicinenet.com
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Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man.
... expressed ClC-7 Cl(-) channel show severe osteopetrosis and retinal degeneration. ... CLCN7 mutations in a patient with human infantile malignant osteopetrosis. ...
http://www.ncbi.nlm.nih.gov/pubmed/11207362
www.ncbi.nlm.nih.gov
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Osteopetrosis and thalamic hypomyelinosis with synaptic degeneration in ...
Osteopetrosis and thalamic hypomyelinosis with synaptic degeneration in DAP12-deficient mice. ... Osteopetrosis/genetics* Receptors, GABA/metabolism ...
http://www.ncbi.nlm.nih.gov/pubmed/12569157?dopt=AbstractPlus
www.ncbi.nlm.nih.gov
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Orphanet: Osteopetrosis
The portal for rare diseases and orphan drugs ... The name osteopetrosis includes various inherited bone disorders characterized ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2781
www.orpha.net
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Osteopetrosis
Important It is possible that the main title of the report Osteopetrosis is not the name you expected. ...
http://www.webmd.com/children/Osteopetrosis
www.webmd.com
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P Drigo - NextBio
Sizes of the terms below reflect their relevance to your search. ... osteomyelitis osteopetrosis preterm infants Rett syndrome SAPHO syndrome Spina ...
http://www.nextbio.com/b/literature/literature.nb?author=P+Drigo
www.nextbio.com
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Talk:Osteopetrosis - Wikipedia, the free encyclopedia
Talk:Osteopetrosis. From Wikipedia, the free encyclopedia. Jump to: navigation, search ... Retrieved from "http://en.wikipedia.org/wiki/Talk:Osteopetrosis" ...
http://en.wikipedia.org/wiki/Talk:Osteopetrosis
en.wikipedia.org
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Orphanet: Osteopetrosis, malignant, autosomal recessive
The portal for rare diseases and orphan drugs ... Osteopetrosis has been reported in most ethnic groups, although, as the disease ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=667
www.orpha.net
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CLCN7-Related Osteopetrosis -- GeneReviews -- NCBI Bookshelf
Bookshelf " GeneReviews " CLCN7-Related Osteopetrosis. Figure 2. ... Copyright © 1993?2009 All Rights Reserved University of Washington, Seattle ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
www.ncbi.nlm.nih.gov
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TCIRG1-dependent recessive osteopetrosis: mutation analysis, functional ...
Human malignant infantile osteopetrosis (arOP) is a genetically heterogeneous ... Osteopetrosis/genetics* Point Mutation. Polymerase Chain Reaction. Protein ...
http://www.ncbi.nlm.nih.gov/pubmed/15300850
www.ncbi.nlm.nih.gov
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interferon Glossary of Terms with Definitions on MedicineNet.com
interferon glossary includes a list of interferon related medical definitions and related links on MedicineNet.com ... See the entire definition of Osteopetrosis ...
http://www.medicinenet.com/interferon/glossary.htm
www.medicinenet.com
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2008 MeSH Tree Structures. C05 - Musculoskeletal Diseases
Home > Library Catalogs and Services > MeSH. MeSH Tree Structures - 2008 ... Osteopetrosis [C05.116.099.708.702.678] Osteopoikilosis [C05.116.099.708.702.685] ...
http://www.nlm.nih.gov/mesh/trees2008/C05.html
www.nlm.nih.gov
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Defects in TCIRG1 subunit of the vacuolar proton pump are responsible ...
Osteopetrosis includes a group of inherited diseases in which inadequate bone ... Infantile malignant autosomal recessive osteopetrosis (MIM 259700) is a severe ...
http://www.ncbi.nlm.nih.gov/pubmed/10888887
www.ncbi.nlm.nih.gov
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The mutational spectrum of human malignant autosomal recessive ...
The mutational spectrum of human malignant autosomal recessive osteopetrosis. ... Human malignant infantile osteopetrosis (arOP; MIM 259700) is a genetically ...
http://www.ncbi.nlm.nih.gov/pubmed/11532986
www.ncbi.nlm.nih.gov
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Chloride channel ClCN7 mutations are responsible for severe recessive ...
... in which a diagnosis of severe osteopetrosis was made within the first 2 years of age. ... 12 cases (13%) of severe osteopetrosis, but only 7 of them had ...
http://www.ncbi.nlm.nih.gov/pubmed/14584882
www.ncbi.nlm.nih.gov
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V-ATPase - Wikipedia, the free encyclopedia
Autosomal dominant osteopetrosis shows mild symptoms in adults who experience ... A form of osteopetrosis that is clinically more severe is termed autosomal ...
http://en.wikipedia.org/wiki/V-ATPase
en.wikipedia.org
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Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile ...
... the gene defects for several mouse mutants with severe osteopetrosis are known, ... Osteopetrosis is thought to be caused by a defect in osteoclast function. ...
http://www.ncbi.nlm.nih.gov/pubmed/10942435
www.ncbi.nlm.nih.gov
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Mechanical properties in long bones of rat osteopetrotic mutations.
Osteopetrosis is a metabolic bone disease with increased skeletal density ... osteopetrotic mutations in the rat (incisors-absent ia/ia, osteopetrosis op ...
http://www.ncbi.nlm.nih.gov/pubmed/11784534?ordinalpos=23&it...
www.ncbi.nlm.nih.gov
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Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal ...
... 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis. ... Osteopetrosis is a heterogeneous group of inherited disorders that includes a ...
http://www.ncbi.nlm.nih.gov/pubmed/12522560
www.ncbi.nlm.nih.gov
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Chloride channel 7 (ClCN7) gene mutations and autosomal dominant ...
... 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II. ... INTRODUCTION: Autosomal dominant osteopetrosis, type II (ADO2) is an uncommon ...
http://www.ncbi.nlm.nih.gov/pubmed/12929941
www.ncbi.nlm.nih.gov
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Novel mutations in the a3 subunit of vacuolar H(+)-adenosine ...
A case of infantile malignant osteopetrosis is described. ... in the TCIRG1 gene in infantile malignant osteopetrosis have been reported in ...
http://www.ncbi.nlm.nih.gov/pubmed/11856654
www.ncbi.nlm.nih.gov
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A splice junction mutation in intron 2 of the carbonic anhydrase II ...
... II gene of osteopetrosis patients from Arabic countries. ... (CA) II deficiency include osteopetrosis, renal tubular acidosis, and cerebral calcification. ...
http://www.ncbi.nlm.nih.gov/pubmed/1301935
www.ncbi.nlm.nih.gov
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Carbonic anhydrase II deficiency identified as the primary defect in ...
... syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification ... one form of inherited osteopetrosis; (ii) provide genetic evidence ...
http://www.ncbi.nlm.nih.gov/pubmed/6405388
www.ncbi.nlm.nih.gov
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Grey-lethal mutation induces severe malignant autosomal recessive ...
... for the development of the most severe autosomal recessive form of osteopetrosis. ... Mutation in the human GL gene leads to severe recessive osteopetrosis. ...
http://www.ncbi.nlm.nih.gov/pubmed/12627228
www.ncbi.nlm.nih.gov
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OSTM1 - Wikipedia, the free encyclopedia
a b "Entrez Gene: OSTM1 osteopetrosis associated transmembrane protein 1" ... Severe malignant osteopetrosis caused by a GL gene mutation.". J. Bone Miner. Res. ...
http://en.wikipedia.org/wiki/OSTM1
en.wikipedia.org
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Identification of a novel mutation in the coding region of the grey ...
Autosomal recessive malignant infantile osteopetrosis (ARO) is characterized by ... analysis of several candidate loci that are involved in murine osteopetrosis. ...
http://www.ncbi.nlm.nih.gov/pubmed/15108279
www.ncbi.nlm.nih.gov
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Pediatrics: Merck Manual Professional
Osteopetrosis with delayed manifestations (Albers-Schönberg disease) Osteopetrosis with precocious manifestations. Osteopetrosis with renal tubular acidosis ...
http://merck.com/mmpe/sec19.html
merck.com
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