Chronic kidney disease in adolescent and adult patients with phenylketonuria
Objectives A lifelong phenylalanine-restricted diet with supplementation of a phenylalanine-free amino acid formula is recommended in patients with phenylketonuria (PKU). The effect of a long-term PKU diet on renal function and blood pressure has not been investigated yet. Design We analyzed renal f...
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Veröffentlicht in: | Journal of inherited metabolic disease 2013-09, Vol.36 (5), p.747-756 |
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creator | Hennermann, Julia B. Roloff, Sylvia Gellermann, Jutta Vollmer, Ilka Windt, Elke Vetter, Barbara Plöckinger, Ursula Mönch, Eberhard Querfeld, Uwe |
description | Objectives
A lifelong phenylalanine-restricted diet with supplementation of a phenylalanine-free amino acid formula is recommended in patients with phenylketonuria (PKU). The effect of a long-term PKU diet on renal function and blood pressure has not been investigated yet.
Design
We analyzed renal function in 67 patients with PKU, aged 15–43 years, by measuring glomerular filtration rate (GFR) and effective renal plasma flow by isotope clearance (
51
Cr-EDTA,
123
J-Hippuran), estimated GFR, blood retention parameters, urinary protein and electrolyte excretion. Renal ultrasound and 24 h ambulatory blood pressure monitoring were performed additionally. Patients were divided into three groups according to their: 1) current diet (CD), i.e., daily protein intake: I
CD
1.04 g/kg; 2) life-long diet time (LDT), i.e., cumulative years of life in which daily protein intake exceeded dietary recommendations: I
LDT
19 years.
Results
GFR was decreased in 19 % of the patients. With increasing protein intake, GFR decreased significantly (I
CD
111 ml/min; II
CD
105 ml/min; III
CD
99 ml/min. I
LDT
112 ml/min; II
LDT
103 ml/min; III
LDT
99 ml/min). Proteinuria was detected in 31 %, microalbuminuria in 7 %, and hypercalciuria in 23 % of the patients. 23 % of the patients had arterial hypertension, and 41 % revealed a nocturnal non-dipping status.
Conclusions
In patients with PKU on a lifelong diet we could detect impaired renal function in 19 %, proteinuria in 31 %, and arterial hypertension in 23 %. Thus, chronic kidney disease may develop in PKU patients, and routine renal function tests should be performed during long-term follow-up. |
doi_str_mv | 10.1007/s10545-012-9548-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1428771907</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3056436491</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4507-74c00cc1066f249ec203ecc5744e36ecaf89e17fa6aa61885b3a31954b923cf43</originalsourceid><addsrcrecordid>eNqFkEuP0zAUhS3EiCkDP4ANioSQ2GS4fsXOEpVXRx2xgbXlOjfUbeoUO1HVfz_upDw0EpqVH_rOveccQl5RuKYA6n2iIIUsgbKylkKX8ITMqFS8ZFUln5IZUEFLXUt5SZ6ntAGAWkv5jFwyTrnO9xlZztexD94VW98EPBaNT2gTFj4Utuk7TA7DUNjQ5OfYDcXeDj7_pOLgh3WxX2M4dlsc-jBGb1-Qi9Z2CV-ezyvy4_On7_Ov5fLbl8X8w7J0QoIqlXAAzlGoqpaJGh0Djs5JJQTyCp1tdY1UtbaytqJayxW3nOaEq5px1wp-Rd5Nc_ex_zViGszOZ6NdZwP2YzJUMK0UrUFl9M0DdNOPMWR39xQHpnWdKTpRLvYpRWzNPvqdjUdDwZyqNlPVJldtTlUbyJrX58njaofNH8XvbjPw9gzY5GzXRhucT385VWnOJc-cmriD7_D4-GZzs7j9CEqcwrFJmbIo_MT4T7j_-r4DwV2lng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1428302889</pqid></control><display><type>article</type><title>Chronic kidney disease in adolescent and adult patients with phenylketonuria</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Springer Nature - Complete Springer Journals</source><creator>Hennermann, Julia B. ; Roloff, Sylvia ; Gellermann, Jutta ; Vollmer, Ilka ; Windt, Elke ; Vetter, Barbara ; Plöckinger, Ursula ; Mönch, Eberhard ; Querfeld, Uwe</creator><creatorcontrib>Hennermann, Julia B. ; Roloff, Sylvia ; Gellermann, Jutta ; Vollmer, Ilka ; Windt, Elke ; Vetter, Barbara ; Plöckinger, Ursula ; Mönch, Eberhard ; Querfeld, Uwe</creatorcontrib><description>Objectives
A lifelong phenylalanine-restricted diet with supplementation of a phenylalanine-free amino acid formula is recommended in patients with phenylketonuria (PKU). The effect of a long-term PKU diet on renal function and blood pressure has not been investigated yet.
Design
We analyzed renal function in 67 patients with PKU, aged 15–43 years, by measuring glomerular filtration rate (GFR) and effective renal plasma flow by isotope clearance (
51
Cr-EDTA,
123
J-Hippuran), estimated GFR, blood retention parameters, urinary protein and electrolyte excretion. Renal ultrasound and 24 h ambulatory blood pressure monitoring were performed additionally. Patients were divided into three groups according to their: 1) current diet (CD), i.e., daily protein intake: I
CD
<0.8 g/kg, II
CD
0.8–1.04 g/kg, III
CD
>1.04 g/kg; 2) life-long diet time (LDT), i.e., cumulative years of life in which daily protein intake exceeded dietary recommendations: I
LDT
<15 years, II
LDT
15–19 years, III
LDT
>19 years.
Results
GFR was decreased in 19 % of the patients. With increasing protein intake, GFR decreased significantly (I
CD
111 ml/min; II
CD
105 ml/min; III
CD
99 ml/min. I
LDT
112 ml/min; II
LDT
103 ml/min; III
LDT
99 ml/min). Proteinuria was detected in 31 %, microalbuminuria in 7 %, and hypercalciuria in 23 % of the patients. 23 % of the patients had arterial hypertension, and 41 % revealed a nocturnal non-dipping status.
Conclusions
In patients with PKU on a lifelong diet we could detect impaired renal function in 19 %, proteinuria in 31 %, and arterial hypertension in 23 %. Thus, chronic kidney disease may develop in PKU patients, and routine renal function tests should be performed during long-term follow-up.</description><identifier>ISSN: 0141-8955</identifier><identifier>EISSN: 1573-2665</identifier><identifier>DOI: 10.1007/s10545-012-9548-0</identifier><identifier>PMID: 23138985</identifier><identifier>CODEN: JIMDDP</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adolescent ; Adult ; Aminoacid disorders ; Biochemistry ; Biological and medical sciences ; Blood Pressure - physiology ; Cross-Sectional Studies ; Diet, Protein-Restricted - adverse effects ; Errors of metabolism ; Female ; Glomerular Filtration Rate - physiology ; Human Genetics ; Humans ; Hypertension - physiopathology ; Internal Medicine ; Kidneys ; Male ; Medical genetics ; Medical sciences ; Medicine ; Medicine & Public Health ; Metabolic Diseases ; Nephrology. Urinary tract diseases ; Original Article ; Pediatrics ; Phenylketonurias - physiopathology ; Phenylketonurias - urine ; Proteinuria - physiopathology ; Proteinuria - urine ; Renal Circulation - physiology ; Renal Insufficiency - physiopathology ; Renal Insufficiency - urine ; Renal Insufficiency, Chronic - urine ; Urinary system involvement in other diseases. Miscellaneous ; Young Adult</subject><ispartof>Journal of inherited metabolic disease, 2013-09, Vol.36 (5), p.747-756</ispartof><rights>SSIEM and Springer Science+Business Media Dordrecht 2012</rights><rights>2013 SSIEM</rights><rights>2014 INIST-CNRS</rights><rights>SSIEM and Springer Science+Business Media Dordrecht 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4507-74c00cc1066f249ec203ecc5744e36ecaf89e17fa6aa61885b3a31954b923cf43</citedby><cites>FETCH-LOGICAL-c4507-74c00cc1066f249ec203ecc5744e36ecaf89e17fa6aa61885b3a31954b923cf43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10545-012-9548-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10545-012-9548-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,41467,42536,45553,45554,51298</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27683353$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23138985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hennermann, Julia B.</creatorcontrib><creatorcontrib>Roloff, Sylvia</creatorcontrib><creatorcontrib>Gellermann, Jutta</creatorcontrib><creatorcontrib>Vollmer, Ilka</creatorcontrib><creatorcontrib>Windt, Elke</creatorcontrib><creatorcontrib>Vetter, Barbara</creatorcontrib><creatorcontrib>Plöckinger, Ursula</creatorcontrib><creatorcontrib>Mönch, Eberhard</creatorcontrib><creatorcontrib>Querfeld, Uwe</creatorcontrib><title>Chronic kidney disease in adolescent and adult patients with phenylketonuria</title><title>Journal of inherited metabolic disease</title><addtitle>J Inherit Metab Dis</addtitle><addtitle>J Inherit Metab Dis</addtitle><description>Objectives
A lifelong phenylalanine-restricted diet with supplementation of a phenylalanine-free amino acid formula is recommended in patients with phenylketonuria (PKU). The effect of a long-term PKU diet on renal function and blood pressure has not been investigated yet.
Design
We analyzed renal function in 67 patients with PKU, aged 15–43 years, by measuring glomerular filtration rate (GFR) and effective renal plasma flow by isotope clearance (
51
Cr-EDTA,
123
J-Hippuran), estimated GFR, blood retention parameters, urinary protein and electrolyte excretion. Renal ultrasound and 24 h ambulatory blood pressure monitoring were performed additionally. Patients were divided into three groups according to their: 1) current diet (CD), i.e., daily protein intake: I
CD
<0.8 g/kg, II
CD
0.8–1.04 g/kg, III
CD
>1.04 g/kg; 2) life-long diet time (LDT), i.e., cumulative years of life in which daily protein intake exceeded dietary recommendations: I
LDT
<15 years, II
LDT
15–19 years, III
LDT
>19 years.
Results
GFR was decreased in 19 % of the patients. With increasing protein intake, GFR decreased significantly (I
CD
111 ml/min; II
CD
105 ml/min; III
CD
99 ml/min. I
LDT
112 ml/min; II
LDT
103 ml/min; III
LDT
99 ml/min). Proteinuria was detected in 31 %, microalbuminuria in 7 %, and hypercalciuria in 23 % of the patients. 23 % of the patients had arterial hypertension, and 41 % revealed a nocturnal non-dipping status.
Conclusions
In patients with PKU on a lifelong diet we could detect impaired renal function in 19 %, proteinuria in 31 %, and arterial hypertension in 23 %. Thus, chronic kidney disease may develop in PKU patients, and routine renal function tests should be performed during long-term follow-up.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aminoacid disorders</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - physiology</subject><subject>Cross-Sectional Studies</subject><subject>Diet, Protein-Restricted - adverse effects</subject><subject>Errors of metabolism</subject><subject>Female</subject><subject>Glomerular Filtration Rate - physiology</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Hypertension - physiopathology</subject><subject>Internal Medicine</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Original Article</subject><subject>Pediatrics</subject><subject>Phenylketonurias - physiopathology</subject><subject>Phenylketonurias - urine</subject><subject>Proteinuria - physiopathology</subject><subject>Proteinuria - urine</subject><subject>Renal Circulation - physiology</subject><subject>Renal Insufficiency - physiopathology</subject><subject>Renal Insufficiency - urine</subject><subject>Renal Insufficiency, Chronic - urine</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Young Adult</subject><issn>0141-8955</issn><issn>1573-2665</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkEuP0zAUhS3EiCkDP4ANioSQ2GS4fsXOEpVXRx2xgbXlOjfUbeoUO1HVfz_upDw0EpqVH_rOveccQl5RuKYA6n2iIIUsgbKylkKX8ITMqFS8ZFUln5IZUEFLXUt5SZ6ntAGAWkv5jFwyTrnO9xlZztexD94VW98EPBaNT2gTFj4Utuk7TA7DUNjQ5OfYDcXeDj7_pOLgh3WxX2M4dlsc-jBGb1-Qi9Z2CV-ezyvy4_On7_Ov5fLbl8X8w7J0QoIqlXAAzlGoqpaJGh0Djs5JJQTyCp1tdY1UtbaytqJayxW3nOaEq5px1wp-Rd5Nc_ex_zViGszOZ6NdZwP2YzJUMK0UrUFl9M0DdNOPMWR39xQHpnWdKTpRLvYpRWzNPvqdjUdDwZyqNlPVJldtTlUbyJrX58njaofNH8XvbjPw9gzY5GzXRhucT385VWnOJc-cmriD7_D4-GZzs7j9CEqcwrFJmbIo_MT4T7j_-r4DwV2lng</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Hennermann, Julia B.</creator><creator>Roloff, Sylvia</creator><creator>Gellermann, Jutta</creator><creator>Vollmer, Ilka</creator><creator>Windt, Elke</creator><creator>Vetter, Barbara</creator><creator>Plöckinger, Ursula</creator><creator>Mönch, Eberhard</creator><creator>Querfeld, Uwe</creator><general>Springer Netherlands</general><general>Springer</general><general>Blackwell Publishing Ltd</general><scope>IQODW</scope><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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>201309</creationdate><title>Chronic kidney disease in adolescent and adult patients with phenylketonuria</title><author>Hennermann, Julia B. ; Roloff, Sylvia ; Gellermann, Jutta ; Vollmer, Ilka ; Windt, Elke ; Vetter, Barbara ; Plöckinger, Ursula ; Mönch, Eberhard ; Querfeld, Uwe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4507-74c00cc1066f249ec203ecc5744e36ecaf89e17fa6aa61885b3a31954b923cf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aminoacid disorders</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - physiology</topic><topic>Cross-Sectional Studies</topic><topic>Diet, Protein-Restricted - adverse effects</topic><topic>Errors of metabolism</topic><topic>Female</topic><topic>Glomerular Filtration Rate - physiology</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Hypertension - physiopathology</topic><topic>Internal Medicine</topic><topic>Kidneys</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic Diseases</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Original Article</topic><topic>Pediatrics</topic><topic>Phenylketonurias - physiopathology</topic><topic>Phenylketonurias - urine</topic><topic>Proteinuria - physiopathology</topic><topic>Proteinuria - urine</topic><topic>Renal Circulation - physiology</topic><topic>Renal Insufficiency - physiopathology</topic><topic>Renal Insufficiency - urine</topic><topic>Renal Insufficiency, Chronic - urine</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hennermann, Julia B.</creatorcontrib><creatorcontrib>Roloff, Sylvia</creatorcontrib><creatorcontrib>Gellermann, Jutta</creatorcontrib><creatorcontrib>Vollmer, Ilka</creatorcontrib><creatorcontrib>Windt, Elke</creatorcontrib><creatorcontrib>Vetter, Barbara</creatorcontrib><creatorcontrib>Plöckinger, Ursula</creatorcontrib><creatorcontrib>Mönch, Eberhard</creatorcontrib><creatorcontrib>Querfeld, Uwe</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of inherited metabolic disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hennermann, Julia B.</au><au>Roloff, Sylvia</au><au>Gellermann, Jutta</au><au>Vollmer, Ilka</au><au>Windt, Elke</au><au>Vetter, Barbara</au><au>Plöckinger, Ursula</au><au>Mönch, Eberhard</au><au>Querfeld, Uwe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic kidney disease in adolescent and adult patients with phenylketonuria</atitle><jtitle>Journal of inherited metabolic disease</jtitle><stitle>J Inherit Metab Dis</stitle><addtitle>J Inherit Metab Dis</addtitle><date>2013-09</date><risdate>2013</risdate><volume>36</volume><issue>5</issue><spage>747</spage><epage>756</epage><pages>747-756</pages><issn>0141-8955</issn><eissn>1573-2665</eissn><coden>JIMDDP</coden><abstract>Objectives
A lifelong phenylalanine-restricted diet with supplementation of a phenylalanine-free amino acid formula is recommended in patients with phenylketonuria (PKU). The effect of a long-term PKU diet on renal function and blood pressure has not been investigated yet.
Design
We analyzed renal function in 67 patients with PKU, aged 15–43 years, by measuring glomerular filtration rate (GFR) and effective renal plasma flow by isotope clearance (
51
Cr-EDTA,
123
J-Hippuran), estimated GFR, blood retention parameters, urinary protein and electrolyte excretion. Renal ultrasound and 24 h ambulatory blood pressure monitoring were performed additionally. Patients were divided into three groups according to their: 1) current diet (CD), i.e., daily protein intake: I
CD
<0.8 g/kg, II
CD
0.8–1.04 g/kg, III
CD
>1.04 g/kg; 2) life-long diet time (LDT), i.e., cumulative years of life in which daily protein intake exceeded dietary recommendations: I
LDT
<15 years, II
LDT
15–19 years, III
LDT
>19 years.
Results
GFR was decreased in 19 % of the patients. With increasing protein intake, GFR decreased significantly (I
CD
111 ml/min; II
CD
105 ml/min; III
CD
99 ml/min. I
LDT
112 ml/min; II
LDT
103 ml/min; III
LDT
99 ml/min). Proteinuria was detected in 31 %, microalbuminuria in 7 %, and hypercalciuria in 23 % of the patients. 23 % of the patients had arterial hypertension, and 41 % revealed a nocturnal non-dipping status.
Conclusions
In patients with PKU on a lifelong diet we could detect impaired renal function in 19 %, proteinuria in 31 %, and arterial hypertension in 23 %. Thus, chronic kidney disease may develop in PKU patients, and routine renal function tests should be performed during long-term follow-up.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>23138985</pmid><doi>10.1007/s10545-012-9548-0</doi><tpages>10</tpages></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Springer Nature - Complete Springer Journals |
subjects | Adolescent Adult Aminoacid disorders Biochemistry Biological and medical sciences Blood Pressure - physiology Cross-Sectional Studies Diet, Protein-Restricted - adverse effects Errors of metabolism Female Glomerular Filtration Rate - physiology Human Genetics Humans Hypertension - physiopathology Internal Medicine Kidneys Male Medical genetics Medical sciences Medicine Medicine & Public Health Metabolic Diseases Nephrology. Urinary tract diseases Original Article Pediatrics Phenylketonurias - physiopathology Phenylketonurias - urine Proteinuria - physiopathology Proteinuria - urine Renal Circulation - physiology Renal Insufficiency - physiopathology Renal Insufficiency - urine Renal Insufficiency, Chronic - urine Urinary system involvement in other diseases. Miscellaneous Young Adult |
title | Chronic kidney disease in adolescent and adult patients with phenylketonuria |
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