Free Online ICD9/ICD9CM Codes And Medical Dictionary Basophilia 288.8. Basophilism (corticoadrenal) (Cushing s) (pituitary) (thymic) 255.0. bassenkornzweig syndrome (abetalipoproteinemia) 272.5. Bat ear 744.29. http://icd9cm.chrisendres.com/index.php?action=alphaletter&letter=Bj
Massachusetts Eye AndEar Infirmary Berman-Gund Laboratory retinitis pigmentosa is a part Usher syndrome, type I and type II; LaurenceMoon-Bardet-Biedl syndrome; bassen-kornzweig syndrome; http://www.meei.harvard.edu/research/labs/bermang.html
Welcome To AJC! s abscess Bartonellosis Bartters syndrome Basal cell cancer Basal cell nevus syndrome Basal ganglia dysfunction bassenkornzweig syndrome Bathing trunk http://www.ajc.com/health/healthfd/shared/health/adam/ency/index/diseidxb.html
Extractions: Subscribe ... Register Now It's Free! Log in E-mail preferences Site Index Search: Site Yellow Pages Customer care ajc.com Nation/World Metro ... Personals ajc services Archives Advertise online Advertise in print Obituaries ... Sitemap Print edition Today This week A1 image E-mail News Sign up for our The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. For further information click here
Health Information Adam Encyclopedia, Basal ganglia dysfunction. Adam Encyclopedia, bassenkornzweig syndrome. Adam Encyclopedia, Bathing trunk nevus. Adam http://www.wregional.com/body.cfm?id=167&action=list&AE_Product_product=ADAMEncy
ENLmedical.com: Conditions And Concerns: Medical Encyclopedia Barium enema Barrett s esophagus Bartholin s abscess Bartter s syndrome Basal cell cancer Basal cell nevus syndrome bassenkornzweig syndrome Bathing trunk http://www.enlmedical.com/Encyc/b.html
RP - 7.3. Englisches Begriffssystem Der RP 1.2.2.1. conerod dystrophy (CRD). 1.2.2.2. abetalipoproteinemia, bassen-kornzweig syndrome. 1.2.2.3. gyrate atrophy. 1.2.2.4. Refsum s disease, Refsum-syndrome. http://www.fask.uni-mainz.de/user/feuerstein/rp/rp-7.3-2.html
Extractions: retinal degenerative disease s, retinal/tapetoretinal degenerations 1.1. acquired forms macular degeneration s through exogenous factors age-related macular degeneration (AMD) 1.2. retinal/tapetoretinal dystrophies, hereditary retinal degenerations 1.2.1. macular dystrophies cystoid macular edema CME ), "wet" form of macular dystrophy (RCD) cone-rod dystrophy (CRD) abetalipoproteinemia Bassen-Kornzweig syndrome 1.2.2.3. gyrate atrophy Refsum's disease Refsum-syndrome Usher's syndrome , Usher-syndrome (US) 1.2.2.5.1. Usher type I (USH1) 1.2.2.5.1.1. Usher type Ia (USH1a) 1.2.2.5.1.2. Usher type Ib (USH1b) 1.2.2.5.1.3. Usher type Ic (USH1C) 1.2.2.5.2. Usher type II (USH2) 1.2.2.5.2.1. Usher type IIa (USH2A) 1.2.2.5.2.2. Usher type IIb (USH2b) 1.2.2.5.3. Usher type III (USH3) 1.2.2.4. other syndromal forms of RP
Chromosome Disorders Also known as bassenkornzweig syndrome. Cri-du-chat Syndrome (Chromosome 5) A disorder of Chromosome 5 which results in multiple congenital anomalies. http://rarediseases.about.com/cs/chromosomeproblem/
Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Types of Diseases Chromosome Disorders Home Essentials Rare Diseases: Basic Information Rare Diseases Support Groups ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Chromosomes hold the genetic keys to all of the body's functions. There may be errors on any of the body's 23 pairs of chromosomes, such as broken or missing pieces or too many pieces or copies. Links below are grouped by chromosome number. Alphabetical Recent Up a category Abetalipoproteinemia Article describes the disorder, its symptoms, diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases. Chromosome 9p Network Provides information, guest book, news, and links.
Abetalipoproteinemia What is it? Abetalipoproteinemia (also known as bassenkornzweig syndrome) is an inherited disorder that affects how fats are made and used in the body. http://rarediseases.about.com/library/weekly/aa072601a.htm
Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Email to a friend Print this page Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. Suggested Reading Internet links on abetalipoproteinemia Elsewhere on the Web Abetalipoproteinemia discussion group Most Popular The Elephant Man's Bones Reveal Mystery ALD and Lorenzo's Oil Prune Belly (Eagle-Barrett) Syndrome Progeria Syndromes ... Mad Cow Disease and Humans What's Hot Christmas Disease Graves' Disease and Research Dystonia and Botox Injections Tourette Syndrome ... Ferraro Fighting Multiple Myeloma From Mary Kugler
Extractions: A disorder of lipid metabolism inherited as an autosomal recessive trait characterized by the near absence of APOLIPOPROTEINS B and apoB-containing lipoproteins in plasma. Microsomal triglyceride transfer protein is deficient or absent in enterocytes. Clinical and laboratory findings include acanthocytosis, hypocholesterolemia, peripheral neuropathy, posterior column degeneration, ataxia, and steatorrhea. Intellectual abilities may also be impaired. (Menkes, Textbook of Child Neurology, 5th ed, p118; Curr Opin Lipidol 1994 Apr;5(2):81-6)
Retinitis Pigmentosa - Questions retardation. bassenkornzweig syndrome (Abetalipoproteineinemia) RP accompanied by progressive neurological problems. Choroideremia http://www.rpsa.org.za/a34.htm
Extractions: RP is just one type of group of inherited diseases that cause degeneration of the retina. Other types include rare syndromes that can usually be diagnosed at a Retinal Clinic. They are generally genetic and follow one of the 3 primary inheritance patterns as mentioned in Number 7. Some of these syndromes are:- Bardet-Biedl (Lawrence-Moon) Syndrome: RP possibly accompanied by physical abnormality, obesity, kidney disease and mental retardation. Bassen-Kornzweig Syndrome (Abetalipoproteineinemia): RP accompanied by progressive neurological problems. Choroideremia: This disease has symptoms similar to Retinitis Pigmentosa but degeneration of both the retina and the choroid occur. Gyrate Atrophy: This disease is associated with a deficiency in the enzyme ornithine Aminotransferase. Myopia, night blindness, cataracts and loss of peripheral vision occur. Leber Congenital Amaurosis: This is characterised by severe visual impairment from birth or very early childhood. Refsum Syndrome: This is a complex disease. Hearing loss, neurological problems, dry or flaky skin can accompany RP. Patients also have oddly shaped red blood cells.
ATAXIA TELANGIECTASIA bassenkornzweig syndrome is another interesting disease that can cause ataxia -and this again is kind of related to something Marvin Ament told you speaking http://www.heartlink.ur.ru/med/10.htm
B In Health > Conditions And Diseases 19); Basilar Migraine@ (4); bassenkornzweig syndrome@ (3); Batten Disease@ (7); Beckwith-Wiedemann Syndrome@ (9); Behcet s Syndrome@ (5 http://ilectric.com/glance/Health/Conditions_and_Diseases/B/
Extractions: Choose a Search Metasearch - The Web Metasearch - This Site Metasearch - News Metasearch - Forums Metasearch - MP3s Metasearch - Code Metasearch - Shopping Directory - Within This Category Only Directory - Entire Category - Arts Category - Business Category - Computers Category - Games Category - Health Category - Home Category - News Category - Recreation Category - Reference Category - Regional Category - Science Category - Shopping Category - Society Category - Sports Category - World Shopping - All products Shopping - Books Shopping - Electronics Shopping - Popular music Shopping - Classical music Shopping - DVD's Shopping - VHS Videos Shopping - In Theaters Shopping - Toys Shopping - Computer Hardware Shopping - Software Shopping - Magazines Shopping - Photo Shopping - Garden / Outdoor Living Shopping - Baby Shopping - Kitchen Lookup - Domain in Whois Lookup - Domain Availability Lookup - HTTP Source Lookup - DNS Record Browse Health Conditions and Diseases B
Book Review The book is organized alphabetically by topic headings, starting and ending with a syndrome abetalipoproteinemia (bassenkornzweig syndrome) as the first http://www.cmj.hr/index.php?P=1248
NIH Guide: THE HEREDITARY ATAXIAS INCLUDING MACHADO-JOSEPH DISEASE telangiectasia, hereditary spastic paraplegia, RoussyLevy and Marinesco-Sjogren syndrome, abetalipoproteinemia (bassen-kornzweig syndrome), Refsum s disease http://grants.nih.gov/grants/guide/pa-files/PA-92-048.html
Classification Of Leukodystrophy And Leukoencephaloencephalopathy Abetalipoproteinemia (bassenkornzweig syndrome). Mutation of alpha-tocopherol transport protein (alpha-TTP) (eg, Ataxia with vitamin E deficiency (AVED). http://moon.ouhsc.edu/kfung/JTY1/NeuroHelp/ZNE2DD01.htm
Extractions: Classification of Leukodystrophy and Leukoencephaloencephalopathy NeuroLearn NeuroHelp Leukodystrophy Definition Leukodystrophy is an umbrellar term that include diseases featured by defective formation and maintenance of myelin. The term leukodystrophy is usually reserved for disorders, often of metabolic origin, characterized by failure in maintenance of myelin. It is, however, a morphological term and not associated with a specific pathologic process or etiology. Classification Leukodystrophies Head X-linked leukodystrophy Autosomal recessive Pattern of inheritance unknown Leukoencephalopath ies Head Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy) Binswanger's disease (subcortical arteriosclerotic encephalopathy) Disseminated necrotizing leukoencephalopathy
Wernicke's Encephalopathy: Features degeneration. The spinocerebellar degeneration can occur as a defect in abetalipoproteins as occurs in bassenkornzweig syndrome. This http://www.rashaduniversity.com/mrashad/werenfeat.html
Product Abstract: Vitamin E (Alpha Tocopherol) ataxia, areflexia, and proprioceptive and vibratory sensory loss, has also been observed in abetalipoproteinemia (bassenkornzweig syndrome), cystic fibrosis http://www.lef.org/prod_hp/abstracts/php-ab426d.html
Extractions: There is increasing evidence that vitamin E is essential for normal neurological function. In abetalipoproteinemia, which is the most severe deficiency state known in man, development of the associated spinocerebellar syndrome can be prevented by early vitamin E therapy. A neurological disorder similar to that seen in abetalipoproteinemia, comprising progressive ataxia, hyporeflexia, and proprioceptive loss, has been described in children and adults with chronic fat malabsorption and vitamin E deficiency. The neuropathological changes in such patients resemble those seen in vitamin E-deficient monkeys. Recent reports suggest that spinocerebellar degeneration may be caused by a selective defect of vitamin E absorption without other evidence of gastrointestinal disease.
