Browsing Health Conditions And Diseases B Category Baillarger Syndrome Balanitis Baldness BardetBiedl Syndrome Barth Syndrome BasalGanglia Diseases Basilar Migraine bassen-kornzweig syndrome Batten Disease http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/B/
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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.
Encyclopædia Britannica The Web's Best Sites, bassenkornzweig syndrome iVillage Notes on this malady,its causes, signs, treatments available, and possible complications. http://www.britannica.com/search?query=cushing's syndrome&ct=igv&fuzzy=N&show=10
Extractions: Anzeige: Verdienen Sie Geld mit Ihren ungenutzten Domains! Welt English Health ... Conditions and Diseases : B A B C D E F ... Eintrag in weiteren Suchmaschinen Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor In einigen Teilen modifizierte Version des DMOZ.
Health Library - Acanthocytosis report. Synonyms. bassenkornzweig syndrome; Low-Density Beta LipoproteinDeficiency. Disorder Subdivisions. None. General Discussion. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=
B Information Sites Diseases@; Basilar Migraine@; bassenkornzweig syndrome@; Batten Disease@;Beckwith-Wiedemann Syndrome@; Behcet's Syndrome@; Bell's Palsy http://healthorgs.com/ConditionsandDiseases/B/
Extractions: King Edward VII Hospital, Windsor, UK. A text for ophthalmologists, outlining the ocular manifestations of systemic diseases. Also for the clinician attempting to diagnose systemic disease. Features icons to point out crucial information, and color photographs on nearly every page. Designed in three-part, sequential format.
IIP-Technologies GmbH - Medizinische Aspekte - Krankheiten Treatable Forms of RP Some rare variations of Retinitis Pigmentosa like Gyrate Atrophy,RefsumSyndrome, bassen-kornzweig syndrome and Abetalipoproteinanemia http://www.iip-tec.com/iip/CMS/2Aspekte3Krankheiten/Files/2002_11_12_14_18_35/Vi
Extractions: Stargardt Disease is the most common form of juvenile Macular Degeneration. Similar to AMD, central vision is affected while peripheral vision remains largely intact. The disease is usually inherited in an autosominal recessive mode which means that both parents carry one healthy and one affected gene each. Only if a child receives two affected genes by the parents (in 25% of the cases) the disease will develop. Best Disease - also known as vitelliform macular dystrophy - is characterized by a loss of central vision similar to other forms of macular degeneration. Usually the disease is diagnosed in childhood. In the initial stages, a bright yellow cyst (fluid-filled sac) forms under the retinal pigment epithelium (RPE) beneath the macula which looks like a sunny-side-up egg. Despite this condition, visual acuity may remain normal or sufficient for many years. In many cases the cyst eventually ruptures which causes further vision loss. However, Best Disease does not always affect both eyes and sometimes it does not progress far enough to cause severe vision loss. The disease follows an autosomal dominant pattern of inheritance so that one affected gene suffices for the condition to develop.
Book Review The book is organized alphabetically by topic headings, starting and ending witha syndrome abetalipoproteinemia (bassenkornzweig syndrome) as the first http://www.cmj.hr/index.php?P=1248
Bassen-Kornzweig (syndrome De) Translate this page bassen-kornzweig (syndrome de). Maladie congénitale, héréditaire, secaractérisant par l'absence de béta-lipoprotéines dans le sang. http://www.vulgaris-medical.com/textb/bassenko.htm
Liste B Translate this page de) Baruk (attaque du gyrus uncinatus de) Baryte Basex (acrokératose paranéoplasique)Basedow (maladie de) bassen-kornzweig (syndrome de) Bassin Bassinet http://www.vulgaris-medical.com/listb.html
RP: Syndrome Und Sonderformen - @med1 bassen-kornzweig-Syndrom(a-ß-Lipoproteinämie); Refsum-Syndrom. Atrophia gyrata. Bei http://www.med1.de/Laien/Krankheiten/Augen/Retinitis.Pigmentosa/Syndrome/
Was Ist RP ? syndrome Usher Syndrom; Atrophiagyrata; bassen-kornzweig-Syndrom (Abetalipoproteinämie); Refsum-Syndrom. http://www.gsi.de/~schuell/rp/was_inh.html
Syndrome Mit Netzhaut-Aderhautdystrophien Translate this page Usher syndrome, Kearns-Sayre Syndrom, Laurence-Moon-Bardet-Biedl Syndrom. Sehrselten Refsum Syndrom, Abetalipoproteinämie (bassen-kornzweig Syndrom). http://retinadiagnostic.de/krank_kell/syndrome_index.html
Fiches Medicales Translate this page MALADIE D'OGUCHI. MALADIE DE bassen-kornzweig - (ABETALIPOPROTEINEMIE).MALADIE DE BECHET. MALADIE DE WAGNER - syndrome DE STICKLER. http://www.retina-france.asso.fr/fiches-medicales.html
Extractions: RETINA FRANCE carte de membre actif ACHROMATOPSIE. ALBINISME. ALTERATION MACULAIRE PAR CONTRACTION D'UNE MEMBRANE EPIRETINIENNE - (SYNDROME DE JAFFE). ALTERATIONS VISUELLES. AMAUROSE CONGENITALE DE LEBER. AMBLYOPIE. ANIRIDIE. ASTIGMATISME. ATAXIE TELANGIECTASIE (TELANGIECTASIES OCULAIRES). ATROPHIES OPTIQUES. CARNICOME BASO-CELLULAIRE DES PAUPIERES. CATARACTE. CATARACTE COMPLIQUEE DANS LA RP. CATARACTE ET LUMIERE. CATARACTE SECONDAIRE. CECITE CORTICALE. CHORIORETINITE SEREUSE CENTRALE (CHORIORETINOPATHIE). CHORIORETINITE TOXOPLASMIQUE (CHORIORETINOPATHIE). CHORIORETINITE VITILIGINEUSE (BIRD-SHOT CHORIORETINOPATHY) (CHORIORETINOPATHIE). CHORIORETINOPATHIES. CHOROIDEREMIE (CHOROIDOSE CHOROIDITE). CHOROIDITE MULTIFOCALE. COLOBOMES. COMPLICATION DE LA MYOPIE DEGENERATIVE. COMPLICATION DU DECOLLEMENT POSTERIEUR DU VITRE PAR COLLAPSUS. COMPLICATIONS OPHTALMOLOGIQUES DE LA MALADIE DE BASEDOW. CORNEA GUTTATA. CORRECTION DE LA MYOPIE PAR LA CHIRURGIE. DECHIRURE RETINIENNE (TROU MACULAIRE). DECOLLEMENT CHOROIDIEN. DECOLLEMENT DE RETINE. DECOLLEMENT DE RETINE PAR TROU MACULAIRE (TRAITEMENT).
Abêtalipoprotéinémie : Sites Et Documents Francophones Translate this page Synonyme(s) bassen-kornzweig, syndrome. Voir aussi apolipoprotéineB . Ne pas confondre avec hypobêtalipoprotéinémie . http://www.chu-rouen.fr/ssf/pathol/abetalipoproteinemie.html
Extractions: Abêtalipoprotéinémie Menu général CISMeF Définition [MeSH Scope Note ; traduction CISMeF] : perturbation héréditaire du métabolisme lipidique caractérisée par la quasi-absence d'apolipoprotéines B et de bêtalipoprotéines dans le plasma. La protéine microsomale de transfert des triglycérides est déficitaire ou absente dans les entérocytes. Les résultats cliniques et de laboratoire incluent acanthocytose, hypocholestérolémie, neuropathie périphérique, dégénération de colonne postérieure, ataxie et stéatorrhée. Les capacités intellectuelles peuvent aussi être diminuées. hémopathies et maladies lymphatiques maladies et malformations congénitales, héréditaires et néonatales métabolisme et nutrition, maladies système nerveux, maladies Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter Ou consulter ci-dessous une sélection des principales ressources :
Svenska RP-föreningen: Refsums Sjukdom Two articles about this disease, clinical description, inheritance, treatment and related diseases Category Health Conditions and Diseases Refsum s bassenkornzweig disease, also known as abetalipoproteinemia, is characterizedby Kearns-Sayre syndrome involves retinal degeneration, ptosis (drooping of http://www.srpf.a.se/forsk/refsum.html
Extractions: Individuals with Refsum disease are unable to metabolize phytanic acid. As a result, high levels of phytanic acid accumulate in blood and tissue. It is thought that disorders associated with this disease result from harmful levels of phytanic acid. Phytanic acid is found in meat, fish, and dairy products. The body also converts phytol, a substance found in green leafy vegetables, to phytanic acid. Refsum disease is usually diagnosed during childhood or young adulthood when vision problems due to RP become apparent. Progressive vision loss from RP begins when harmful levels of phytanic acid collect beneath the retina. The retina is essential to vision as it converts light into electrical impulses and then transfers these impulses to the brain via the optic nerve. The first symptom of RP is night blindness followed by a gradual loss of peripheral (side) vision. Night blindness makes vision difficult in dark or dimly lit places. The loss of peripheral vision is often referred to as tunnel vision. RP tends to progress slowly in patients with Refsum disease.
Birth Disorder Information Directory - A Deficiency/Defect Anomalad/syndrome See Prune Belly syndrome. Abetalipoproteinemia(Bassen Kornzweig syndrome) List of Sites. Ablepharon http://www.bdid.com/defectaa.htm
Extractions: HOME Aagenaes Syndrome (Cholestasis-Lymphedema Syndrome) Aarskog (Scott) Syndrome (Faciodigitogenital Syndrome, Faciogenital Dysplasia) Aarskog-Like Syndrome (Faciodigitogenital Syndrome, Recessive Form; Teebi Naguib Alawadi Syndrome) Aarskog Ose Pande Syndrome (Lipodystrophy Rieger Anomaly Diabetes) AASE Syndrome (Anemia with Triphalangeal Thumbs) AASE Smith Syndrome (Hydrocephalus with Cleft Palate and Joint Contractures) ABCD Syndrome (Albinism, Black Lock, Cell Migration Disorder of the Neurocytes of the Gut, and Deafness) Abdallat Davis Farrage Syndrome (Neurocutaneous Syndrome, Abdallat Type; Spastic Paraplegia-Pigmentary Abnormalities) Abdominal Muscle Absence/Aplasia/Deficiency/Defect Anomalad/Syndrome Abetalipoproteinemia (Bassen Kornzweig Syndrome) Ablepharon -Macrostomia Syndrome Allison has AMS (Has a photo gallery)
