A study of the renal handling and intestinal absorption of dibasic amino acids in a patient with genotype +/11 heterozygous cystinuria and idiopathic hypercalcuria
A case is reported of a patient with idiopathic hypercalcuria who was referred for investigation of renal calculi. Studies of urinary amino acid excretion in the patient and all living members of his family, as well as studies of endogenous renal clearances of dibasic amino acids and cystine in the...
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| Veröffentlicht in: | Clinica chimica acta 1975-03, Vol.59 (2), p.195-201 |
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| container_title | Clinica chimica acta |
| container_volume | 59 |
| creator | Silk, D.B.A. Perrett, D. Clark, M.L. Stephens, A.D. Scowen, E.F. |
| description | A case is reported of a patient with idiopathic hypercalcuria who was referred for investigation of renal calculi. Studies of urinary amino acid excretion in the patient and all living members of his family, as well as studies of endogenous renal clearances of dibasic amino acids and cystine in the patient and his daughter, indicated that the patient had genotype +/11 heterozygous cystinuria. Intestinal perfusion studies showed however that the patient was able to absorb
l-lysine,
l-arginine normally from the jejunum and ileum. This suggests that a difference exists between renal and intestinal handling of lysine and arginine in cystinuria. |
| doi_str_mv | 10.1016/0009-8981(75)90029-7 |
| format | Article |
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l-lysine,
l-arginine normally from the jejunum and ileum. This suggests that a difference exists between renal and intestinal handling of lysine and arginine in cystinuria.</description><identifier>ISSN: 0009-8981</identifier><identifier>EISSN: 1873-3492</identifier><identifier>DOI: 10.1016/0009-8981(75)90029-7</identifier><identifier>PMID: 1120363</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Amino Acids, Diamino - metabolism ; Calcium - metabolism ; Calcium - urine ; Cystinuria - metabolism ; Genotype ; Heterozygote ; Humans ; Ileum - metabolism ; Intestinal Absorption ; Jejunum - metabolism ; Kidney - metabolism ; Kidney Calculi ; Male ; Metal Metabolism, Inborn Errors - metabolism</subject><ispartof>Clinica chimica acta, 1975-03, Vol.59 (2), p.195-201</ispartof><rights>1975</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-30f130655dc122f323797712f076a9fa879cf7622dda351d00451c4b25a350833</citedby><cites>FETCH-LOGICAL-c357t-30f130655dc122f323797712f076a9fa879cf7622dda351d00451c4b25a350833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0009898175900297$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1120363$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silk, D.B.A.</creatorcontrib><creatorcontrib>Perrett, D.</creatorcontrib><creatorcontrib>Clark, M.L.</creatorcontrib><creatorcontrib>Stephens, A.D.</creatorcontrib><creatorcontrib>Scowen, E.F.</creatorcontrib><title>A study of the renal handling and intestinal absorption of dibasic amino acids in a patient with genotype +/11 heterozygous cystinuria and idiopathic hypercalcuria</title><title>Clinica chimica acta</title><addtitle>Clin Chim Acta</addtitle><description>A case is reported of a patient with idiopathic hypercalcuria who was referred for investigation of renal calculi. Studies of urinary amino acid excretion in the patient and all living members of his family, as well as studies of endogenous renal clearances of dibasic amino acids and cystine in the patient and his daughter, indicated that the patient had genotype +/11 heterozygous cystinuria. Intestinal perfusion studies showed however that the patient was able to absorb
l-lysine,
l-arginine normally from the jejunum and ileum. This suggests that a difference exists between renal and intestinal handling of lysine and arginine in cystinuria.</description><subject>Adult</subject><subject>Amino Acids, Diamino - metabolism</subject><subject>Calcium - metabolism</subject><subject>Calcium - urine</subject><subject>Cystinuria - metabolism</subject><subject>Genotype</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Ileum - metabolism</subject><subject>Intestinal Absorption</subject><subject>Jejunum - metabolism</subject><subject>Kidney - metabolism</subject><subject>Kidney Calculi</subject><subject>Male</subject><subject>Metal Metabolism, Inborn Errors - metabolism</subject><issn>0009-8981</issn><issn>1873-3492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1975</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uctq3TAQFaEhvU3yByloVVqKGz2uLWtTCKGPQCCbZi10Jfl6iq_kSnKL8zv90chxaHdZDaPzGM0ZhC4o-UQJbS4JIbJqZUvfi_qDJITJShyhDW0Fr_hWsldo84_yGr1J6Wdpt6ShJ-iEUkZ4wzfo7xVOebIzDh3OvcPReT3gXns7gN_jUjH47FKG5V3vUohjhuAXvoWdTmCwPoAPWBuwqZCxxqPO4HzGfyD3eO98yPPo8MdLSnHvsovhYd6HKWEzL75TBL0OshCKtC-WfRFEowezgGfouNNDcufP9RTdf_3y4_p7dXv37eb66rYyvBa54qSjnDR1bQ1lrOOMCykEZR0RjZadboU0nWgYs1bzmtoSRk3Ndsfq0pKW81P0bvUdY_g1lZ3VAZJxw6C9K99VLROScNYW4nYlmhhSiq5TY4SDjrOiRC23UUvwagleiVo93UaJInv77D_tDs7-F63HKPjnFXdlyd_gokqm5GichehMVjbAywMeAcmln48</recordid><startdate>19750310</startdate><enddate>19750310</enddate><creator>Silk, D.B.A.</creator><creator>Perrett, D.</creator><creator>Clark, M.L.</creator><creator>Stephens, A.D.</creator><creator>Scowen, E.F.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19750310</creationdate><title>A study of the renal handling and intestinal absorption of dibasic amino acids in a patient with genotype +/11 heterozygous cystinuria and idiopathic hypercalcuria</title><author>Silk, D.B.A. ; Perrett, D. ; Clark, M.L. ; Stephens, A.D. ; Scowen, E.F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-30f130655dc122f323797712f076a9fa879cf7622dda351d00451c4b25a350833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><topic>Adult</topic><topic>Amino Acids, Diamino - metabolism</topic><topic>Calcium - metabolism</topic><topic>Calcium - urine</topic><topic>Cystinuria - metabolism</topic><topic>Genotype</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Ileum - metabolism</topic><topic>Intestinal Absorption</topic><topic>Jejunum - metabolism</topic><topic>Kidney - metabolism</topic><topic>Kidney Calculi</topic><topic>Male</topic><topic>Metal Metabolism, Inborn Errors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silk, D.B.A.</creatorcontrib><creatorcontrib>Perrett, D.</creatorcontrib><creatorcontrib>Clark, M.L.</creatorcontrib><creatorcontrib>Stephens, A.D.</creatorcontrib><creatorcontrib>Scowen, E.F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silk, D.B.A.</au><au>Perrett, D.</au><au>Clark, M.L.</au><au>Stephens, A.D.</au><au>Scowen, E.F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A study of the renal handling and intestinal absorption of dibasic amino acids in a patient with genotype +/11 heterozygous cystinuria and idiopathic hypercalcuria</atitle><jtitle>Clinica chimica acta</jtitle><addtitle>Clin Chim Acta</addtitle><date>1975-03-10</date><risdate>1975</risdate><volume>59</volume><issue>2</issue><spage>195</spage><epage>201</epage><pages>195-201</pages><issn>0009-8981</issn><eissn>1873-3492</eissn><abstract>A case is reported of a patient with idiopathic hypercalcuria who was referred for investigation of renal calculi. Studies of urinary amino acid excretion in the patient and all living members of his family, as well as studies of endogenous renal clearances of dibasic amino acids and cystine in the patient and his daughter, indicated that the patient had genotype +/11 heterozygous cystinuria. Intestinal perfusion studies showed however that the patient was able to absorb
l-lysine,
l-arginine normally from the jejunum and ileum. This suggests that a difference exists between renal and intestinal handling of lysine and arginine in cystinuria.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>1120363</pmid><doi>10.1016/0009-8981(75)90029-7</doi><tpages>7</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0009-8981 |
| ispartof | Clinica chimica acta, 1975-03, Vol.59 (2), p.195-201 |
| issn | 0009-8981 1873-3492 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_82790328 |
| source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
| subjects | Adult Amino Acids, Diamino - metabolism Calcium - metabolism Calcium - urine Cystinuria - metabolism Genotype Heterozygote Humans Ileum - metabolism Intestinal Absorption Jejunum - metabolism Kidney - metabolism Kidney Calculi Male Metal Metabolism, Inborn Errors - metabolism |
| title | A study of the renal handling and intestinal absorption of dibasic amino acids in a patient with genotype +/11 heterozygous cystinuria and idiopathic hypercalcuria |
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