¿qué es 'Síndrome de Bardet-Biedl - trastorno genético con la obesidad y el hipogonadismo '? Definición de Síndrome de Bardet-Biedl The Bardet-Biedl syndrome is a genetic disorder characterized mainly by obesity, pigmentary retinopathy, polydactyly, mental retardation, hypogonadism, and renal failure in some cases. do i have 'Síndrome de Bardet-Biedl'? Además las siguientes pruebas de diagnóstico puede ser necesario para ayudar a verificar el diagnóstico: prueba de diagnóstico de los resultados de la búsqueda 'Síndrome de Bardet-Biedl' 1 - 5 of 10 pruebas de diagnóstico Los estudios de genética molecular Síndrome de Bardet-Biedl y Los estudios de genética molecular BUN Síndrome de Bardet-Biedl y BUN Serum Creatinine Síndrome de Bardet-Biedl y Serum Creatinine Ecografía renal uréter vejiga Síndrome de Bardet-Biedl y Ecografía renal uréter vejiga Análisis de orina Examination of urine to detect disease Síndrome de Bardet-Biedl y Análisis de orina electrolitos séricos Síndrome de Bardet-Biedl y electrolitos séricos CT riñones Síndrome de Bardet-Biedl y CT riñones CT scan Síndrome de Bardet-Biedl y CT scan Comprehensive eye exam Síndrome de Bardet-Biedl y Comprehensive eye exam Developmental testing Síndrome de Bardet-Biedl y Developmental testing para obtener más ingreso por favor, es de acceso libre (haga clic aquí para acceder) procedimientos terapéuticos para 'Síndrome de Bardet-Biedl'? La gestión o tratamiento de enfermedades debe ser siempre determinada por un proveedor de servicios de salud los pacientes. Abajo hay una lista de asociados procedimientos terapéuticos o medicamentos para Bardet-Biedl Syndrome: procedimiento terapéutico de los resultados de la búsqueda 'Síndrome de Bardet-Biedl' rankings are computer generated. por favor consulte a su proveedor de servicios de salud. medicamentos para los resultados de la búsqueda 'Síndrome de Bardet-Biedl' 1 - 1 of 1 medicamentos rankings are computer generated. por favor consulte a su proveedor de servicios de salud.   insulina Síndrome de Bardet-Biedl y insulina resultados de la búsqueda web para 'Síndrome de Bardet-Biedl'? Web (All)  |  Tratamiento  |  Droga  |  Pruebas  |  Investigación  |  Dieta Resultados 1 - 50 - Síndrome de Bardet-Biedl Bardet-Biedl syndrome - Wikipedia, the free encyclopedia [Traducir esta página] The Bardet-Biedl syndrome is a ciliopathic human genetic disorder that produces ... Laurence-Moon-Biedl-Bardet syndrome are no longer considered as valid terms in ... http://en.wikipedia.org/wiki/Bardet-Biedl_syndrome   en.wikipedia.org - summary Bardet-Biedl syndrome 4 (BBS4) [Traducir esta página] Homo sapiens Bardet-Biedl syndrome 4 splice variant 1 (BBS4) mRNA, complete cds, ... Homo sapiens Bardet-Biedl syndrome 4, mRNA (cDNA clone IMAGE:3659371) ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=208681   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 1 (BBS1) [Traducir esta página] Homo sapiens Bardet-Biedl syndrome 1, mRNA (cDNA clone MGC: ... Homo sapiens cDNA FLJ54009 complete cds, highly similar to Bardet-Biedl syndrome 1 protein ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=502915   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 7 (Bbs7) [Traducir esta página] Norway rat protein-coding gene Bbs7. Represented by 19 ESTs from 15 cDNA libraries. ... Rattus norvegicus Bardet-Biedl syndrome 7, mRNA (cDNA clone MGC:94101 IMAGE: ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=28442   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Bardet-Biedl syndrome (BBS) is characterized by cone-rod dystrophy, truncal ... Bardet-Biedl syndrome is inherited in an autosomal recessive manner. ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bbs   www.ncbi.nlm.nih.gov - summary [Bardet-Biedl syndrome] [Traducir esta página] Bardet-Biedl syndrome (BBS) is a ciliopathy causing multivisceral abnormalities. ... Bardet-Biedl Syndrome/pathology* Diagnosis, Differential. Genetic ... http://www.ncbi.nlm.nih.gov/pubmed/19019343?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 2 (bbs2) [Traducir esta página] Zebrafish protein-coding gene bbs2. Represented by 15 ESTs ... Danio rerio Bardet-Biedl syndrome 2, mRNA (cDNA clone MGC:73041 IMAGE:4786691), complete cds ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Dr&CID=1599   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 5 (BBS5) [Traducir esta página] Homo sapiens Bardet-Biedl syndrome protein 5 isoform 2 (BBS5) mRNA, complete cds ... FLJ60989 complete cds, highly similar to Bardet-Biedl syndrome 5 protein ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=233398   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 12 (BBS12) [Traducir esta página] Human protein-coding gene BBS12. Represented by 115 ESTs from 68 cDNA libraries. ... Homo sapiens Bardet-Biedl syndrome 12, mRNA (cDNA clone IMAGE:4327935), with ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=400698   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 7 (BBS7) [Traducir esta página] Human protein-coding gene BBS7. Represented by 139 ESTs from ... Homo sapiens Bardet-Biedl syndrome 7, mRNA (cDNA clone MGC:45066 IMAGE:5240398), complete cds ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=591694   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 9 (BBS9) [Traducir esta página] Homo sapiens Bardet-Biedl syndrome 9 (BBS9), transcript variant 2, mRNA ... Homo sapiens Bardet-Biedl syndrome 9, mRNA (cDNA clone IMAGE:5519851), complete cds ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=372360   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 10 (BBS10) [Traducir esta página] Human protein-coding gene BBS10. Represented by 120 ESTs from 63 cDNA libraries. ... Homo sapiens Bardet-Biedl syndrome 10, mRNA (cDNA clone IMAGE:3919095), complete ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&MAXEST=999999&CID=96322   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 5 (human) (Bbs5) [Traducir esta página] PREDICTED: similar to Bardet-Biedl syndrome 5 isoform 3. C. lupus ... Mus musculus Bardet-Biedl syndrome 5 (human), mRNA (cDNA clone MGC:74138 IMAGE: ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=252136   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 2 (human) (Bbs2) [Traducir esta página] Mouse protein-coding gene Bbs2. Represented by 71 ESTs from 47 cDNA libraries. ... Mus musculus Bardet-Biedl syndrome 2 (human), mRNA (cDNA clone MGC:67844 IMAGE: ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=292107   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 10. BBS7 Pathologic Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 3. BBS1 Pathologic Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary MKKS - McKusick-Kaufman syndrome - Genetics Home Reference [Traducir esta página] More than 20 MKKS mutations have been found to cause Bardet-Biedl syndrome. ... MKKS protein leads to the characteristic features of Bardet-Biedl syndrome. ... http://ghr.nlm.nih.gov/gene=mkks   ghr.nlm.nih.gov - summary Bardet-Biedl syndrome 2 (BBS2) [Traducir esta página] ... sapiens mRNA for Bardet-Biedl syndrome 2 protein variant ... Homo sapiens Bardet-Biedl syndrome 2, mRNA (cDNA clone MGC:20703 IMAGE:4653315), complete cds ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=333738   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 1 (human) (Bbs1) [Traducir esta página] Mouse protein-coding gene Bbs1. Represented by 93 ESTs from 57 cDNA ... Mus musculus Bardet-Biedl syndrome 1 homolog (human), mRNA (cDNA clone IMAGE:30619127) ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=23636   www.ncbi.nlm.nih.gov - summary National Library of Medicine [Traducir esta página] A summary of Bardet-Biedl syndrome and a list of major features. http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome048.html   www.nlm.nih.gov - summary Bardet-Biedl syndrome 7 (human) (Bbs7) [Traducir esta página] Mouse protein-coding gene Bbs7. Represented by 127 ESTs from 57 cDNA libraries. ... Mus musculus Bardet-Biedl syndrome 7 (human), mRNA (cDNA clone MGC:27874 IMAGE: ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=286187   www.ncbi.nlm.nih.gov - summary Alström syndrome - Wikipedia, the free encyclopedia [Traducir esta página] Alstrom syndrome is sometimes confused with Bardet-Biedl syndrome, which has similar symptoms. Bardet-Biedl syndrome tends to have later onset in its symptoms. ... http://en.wikipedia.org/wiki/Alstrom_syndrome   en.wikipedia.org - summary Bardet-Biedl syndrome 2 homolog (human) (Bbs2) [Traducir esta página] Norway rat protein-coding gene Bbs2. Represented by 38 ESTs from 31 cDNA libraries. ... Rattus norvegicus Bardet-Biedl syndrome 2 homolog (human) (Bbs2), mRNA. P ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=15987   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 7. BBS4 Pathologic Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 9. MKKS/BBS6 Pathologic Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary Bardet Biedl Syndrome - Yahoo! Health [Traducir esta página] Important It is possible that the main title of the report Bardet Biedl Syndrome is not the name you expected. Please check the synonyms listing to find the ... http://health.yahoo.com/vision-resources/bardet-biedl-syndro...   health.yahoo.com - summary Mutations in MKKS cause Bardet-Biedl syndrome. [Traducir esta página] Bardet-Biedl syndrome (BBS) is an autosomal recessive disorder with locus heterogeneity. ... Bardet-Biedl Syndrome/diagnosis. Bardet-Biedl Syndrome/genetics ... http://www.ncbi.nlm.nih.gov/pubmed/10973238   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 4 (human) (Bbs4) [Traducir esta página] bardet biedl syndrome 4 protein. C. reinhardtii. 58.7. 397. GENE ... Mus musculus Bardet-Biedl syndrome 4 (human), mRNA (cDNA clone IMAGE:6413148), partial cds ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=200714   www.ncbi.nlm.nih.gov - summary McKusick-Kaufman syndrome - Genetics Home Reference [Traducir esta página] Bardet-Biedl syndrome has several features that are not seen in McKusick-Kaufman ... been diagnosed with the disorder were later found to have Bardet-Biedl syndrome. ... http://ghr.nlm.nih.gov/condition=mckusickkaufmansyndrome   ghr.nlm.nih.gov - summary Bardet-Biedl syndrome 9 (human) (Bbs9) [Traducir esta página] Mouse protein-coding gene Bbs9. Represented by 142 ESTs from 69 ... Mus musculus Bardet-Biedl syndrome 9 (human), mRNA (cDNA clone IMAGE:6468740), complete cds ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=176725   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 12 (human) (Bbs12) [Traducir esta página] Mouse protein-coding gene Bbs12. Represented by 22 ESTs from 9 cDNA libraries. ... Mus musculus Bardet-Biedl syndrome 12 (human), mRNA (cDNA clone IMAGE:30540467) PA ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=32171   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 5 (human) (Bbs5) [Traducir esta página] BBS (Bardet-Biedl Syndrome) protein family member (bbs-5) C. elegans. 48.1 ... Rattus norvegicus Bardet-Biedl syndrome 5 (human), mRNA (cDNA clone MGC:189245 ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=45505   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 8. MKKS/BBS6 Normal Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 4. BBS2 Normal Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome: beyond the cilium. [Traducir esta página] Bardet-Biedl syndrome: beyond the cilium. Tobin JL, Beales PL. ... The Bardet-Biedl syndrome (BBS) is a significant genetic cause of chronic and ... http://www.ncbi.nlm.nih.gov/pubmed/17357787   www.ncbi.nlm.nih.gov - summary Laurence-Moon syndrome - Wikipedia, the free encyclopedia [Traducir esta página] ... and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year ... Laurence-Moon-Bardet-Biedl Syndrome. Medical notes and references. v ? d ? e ... http://en.wikipedia.org/wiki/Laurence_Moon_syndrome   en.wikipedia.org - summary BBS2(BBS) - NextBio [Traducir esta página] BBS: This gene encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome ... http://www.nextbio.com/b/home/home.nb?q=BBS   www.nextbio.com - summary Bardet-Biedl syndrome 1 homolog (human) (Bbs1) [Traducir esta página] Norway rat protein-coding gene Bbs1. Represented by 40 ESTs from 28 cDNA libraries. ... Rattus norvegicus Bardet-Biedl syndrome 1 homolog (human) (Bbs1), mRNA. P ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=12497&log$=unigeneTable   www.ncbi.nlm.nih.gov - summary Möbius syndrome - Wikipedia, the free encyclopedia [Traducir esta página] Möbius syndrome (also spelled Moebius) is an extremely rare congenital ... Laurence-Moon-Bardet-Biedl. Bardet-Biedl syndrome · Laurence-Moon syndrome. Combined/other, ... http://en.wikipedia.org/wiki/M%C3%B6bius_syndrome   en.wikipedia.org - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 6. BBS4 Normal Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary Bardet-Biedl Syndrome -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Search for. Within This book All books PubMed. Bookshelf " GeneReviews " Bardet-Biedl Syndrome. Table 5. BBS2 Pathologic Allelic Variants ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...   www.ncbi.nlm.nih.gov - summary New criteria for improved diagnosis of Bardet-Biedl syndrome: results ... [Traducir esta página] ... for improved diagnosis of Bardet-Biedl syndrome: results of a population ... Bardet-Biedl syndrome (BBS) is an autosomal recessive condition characterised by ... http://www.ncbi.nlm.nih.gov/pubmed/10874630   www.ncbi.nlm.nih.gov - summary Identification of a Bardet-Biedl syndrome locus on chromosome 3 and ... [Traducir esta página] Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation ... Bardet-Biedl syndrome is an autosomal recessive disorder characterized by mental ... http://www.ncbi.nlm.nih.gov/pubmed/7987310   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome 4 homolog (human) (Bbs4) [Traducir esta página] bardet biedl syndrome 4 protein. C. reinhardtii. 54.7. 397. GENE EXPRESSION ... Rattus norvegicus Bardet-Biedl syndrome 4 homolog (human) (Bbs4), mRNA. PA ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Rn&CID=25002   www.ncbi.nlm.nih.gov - summary Fountain syndrome - Wikipedia, the free encyclopedia [Traducir esta página] Beckwith-Wiedemann syndrome · Sotos syndrome · Weaver syndrome. Laurence-Moon-Bardet-Biedl. Bardet-Biedl syndrome · Laurence-Moon syndrome. Combined/other, ... http://en.wikipedia.org/wiki/Fountain_syndrome   en.wikipedia.org - summary Bardet-Biedl syndrome 10 (human) (Bbs10) [Traducir esta página] Mouse protein-coding gene Bbs10. Represented by 17 ESTs from ... PREDICTED: Mus musculus Bardet-Biedl syndrome 10 (human), transcript variant 1 (Bbs10), mRNA ... http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Mm&CID=45256   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome: a case report. [Traducir esta página] ... J. 2008 Jan 15;14(1):9. Bardet-Biedl syndrome: a case report. Karaman A. ... Bardet-Biedl syndrome (BBS) is a genetically heterogeneous autosomal recessive ... http://www.ncbi.nlm.nih.gov/pubmed/18319026   www.ncbi.nlm.nih.gov - summary Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families. [Traducir esta página] ... autosomal recessive disorder Bardet-Biedl syndrome is characterised by retinal ... genes responsible for Bardet-Biedl syndrome may influence growth ... http://www.ncbi.nlm.nih.gov/pubmed/9039982   www.ncbi.nlm.nih.gov - summary Dubowitz syndrome - Wikipedia, the free encyclopedia [Traducir esta página] Dubowitz syndrome is a rare genetic disorder characterized by ... Laurence-Moon-Bardet-Biedl. Bardet-Biedl syndrome · Laurence-Moon syndrome. Combined/other, ... http://en.wikipedia.org/wiki/Dubowitz_syndrome   en.wikipedia.org - summary Bardet-Biedl syndrome: an emerging pathomechanism of intracellular ... [Traducir esta página] Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport. ... been made in understanding the genetic and molecular aetiology of Bardet-Biedl ... http://www.ncbi.nlm.nih.gov/pubmed/16909204   www.ncbi.nlm.nih.gov - summary mostrar más 1  2

Chat with eNurse Kim about 'Síndrome de Bardet-Biedl' or something else! búsqueda rápida categoría genética o congénita frecuencia raro (U.S.) riesgo por edad riesgo por la duración de los síntomas algunos síntomas comunes ausente púbico y axilar cabello deformidad de la nariz adicional o dedos y dedos de los pies obesos algunos relacionados con los diagnósticos o labio leporino y paladar Síndrome de Carpenter Síndrome de Laurence-Moon Síndrome de Apert más related physician types family practitioner internist genetics specialist show local physicians código postal Buscar local Los resultados generados por computadora son sugerencias para ayudarle a encontrar un médico. MEDgle no recomienda ningún tipo de médico o pretenden ser completos o precisos en los proveedores y sugirió especialidades.