De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease
Mutations in the gene encoding the transcription factor hepatocyte nuclear factor (HNF)-1 beta are associated with maturity-onset diabetes of the young (type V), non-diabetic renal disease, and occasionally genital malformations in females. Recently, familial hypoplastic glomerulocystic kidney disea...
Gespeichert in:
Veröffentlicht in: | Pediatric nephrology (Berlin, West) West), 2002-12, Vol.17 (12), p.1021-1026 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1026 |
---|---|
container_issue | 12 |
container_start_page | 1021 |
container_title | Pediatric nephrology (Berlin, West) |
container_volume | 17 |
creator | Mache, Christoph J Preisegger, Karl-Heinz Kopp, Susanne Ratschek, Manfred Ring, Ekkehard |
description | Mutations in the gene encoding the transcription factor hepatocyte nuclear factor (HNF)-1 beta are associated with maturity-onset diabetes of the young (type V), non-diabetic renal disease, and occasionally genital malformations in females. Recently, familial hypoplastic glomerulocystic kidney disease (GCKD) has been added to the clinical spectrum of HNF-1 beta gene mutations. Familial hypoplastic GCKD is a rare, dominantly inherited disorder characterized by small kidneys containing glomerular cysts, abnormal pelvicalyceal anatomy, and chronic renal failure. A family with hypoplastic GCKD occurring in the father and the daughter was screened for mutations in the HNF-1 beta gene. The sequence of exon 4 of the HNF-1 beta gene revealed a C insertion at codon 334 resulting in a frameshift mutation (P334fsinsC) in two family members. The P334fsinsC allele co-segregated with hypoplastic GCKD in the family. Oral glucose tolerance testing was normal in the 11-year-old girl. In her 38-year-old father, impaired glucose tolerance was detected. These studies provide further evidence that familial hypoplastic GCKD is associated with HNF-1 beta gene mutations. HNF-1 beta gene mutation screening may prove useful in patients with small cystic kidneys and chronic renal failure, in whom a definite renal diagnosis could otherwise only be established by renal biopsy. |
doi_str_mv | 10.1007/s00467-002-0975-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72762855</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72762855</sourcerecordid><originalsourceid>FETCH-LOGICAL-c297t-218dc1f0b82649ece18a83586728df5e55be414a3f7dfe15a5a56480f2638483</originalsourceid><addsrcrecordid>eNpFkDFPwzAUhD2AaCn8ABbkic1gO3bsjKhQilTBUgk2y0meiyGJQ5wg5d-T0krohqeT7k5PH0JXjN4yStVdpFSkilDKCc2UJPwEzWmWMEIFe5-h8xg_KaVa6vQMzRgXSieSzdHbA-Am_AS8flkRhnPoLd5BA7geetv70GDfYGdrX3lb4Y-xDW1lY-8LvKtCDd1QhWL881--bGDEpY9gI1ygU2erCJfHu0Db1eN2uSab16fn5f2GFDxTPeFMlwVzNNc8FRkUwLSdHtOp4rp0EqTMQTBhE6dKB0zaSanQ1PE00UInC3RzmG278D1A7E3tYwFVZRsIQzSKq5RrKacgOwSLLsTYgTNt52vbjYZRswdoDgDNBNDsARo-da6P40NeQ_nfONJLfgEXXG2x</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72762855</pqid></control><display><type>article</type><title>De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Mache, Christoph J ; Preisegger, Karl-Heinz ; Kopp, Susanne ; Ratschek, Manfred ; Ring, Ekkehard</creator><creatorcontrib>Mache, Christoph J ; Preisegger, Karl-Heinz ; Kopp, Susanne ; Ratschek, Manfred ; Ring, Ekkehard</creatorcontrib><description>Mutations in the gene encoding the transcription factor hepatocyte nuclear factor (HNF)-1 beta are associated with maturity-onset diabetes of the young (type V), non-diabetic renal disease, and occasionally genital malformations in females. Recently, familial hypoplastic glomerulocystic kidney disease (GCKD) has been added to the clinical spectrum of HNF-1 beta gene mutations. Familial hypoplastic GCKD is a rare, dominantly inherited disorder characterized by small kidneys containing glomerular cysts, abnormal pelvicalyceal anatomy, and chronic renal failure. A family with hypoplastic GCKD occurring in the father and the daughter was screened for mutations in the HNF-1 beta gene. The sequence of exon 4 of the HNF-1 beta gene revealed a C insertion at codon 334 resulting in a frameshift mutation (P334fsinsC) in two family members. The P334fsinsC allele co-segregated with hypoplastic GCKD in the family. Oral glucose tolerance testing was normal in the 11-year-old girl. In her 38-year-old father, impaired glucose tolerance was detected. These studies provide further evidence that familial hypoplastic GCKD is associated with HNF-1 beta gene mutations. HNF-1 beta gene mutation screening may prove useful in patients with small cystic kidneys and chronic renal failure, in whom a definite renal diagnosis could otherwise only be established by renal biopsy.</description><identifier>ISSN: 0931-041X</identifier><identifier>DOI: 10.1007/s00467-002-0975-2</identifier><identifier>PMID: 12478351</identifier><language>eng</language><publisher>Germany</publisher><subject>Austria ; DNA - biosynthesis ; DNA - genetics ; DNA-Binding Proteins ; Female ; Frameshift Mutation - genetics ; Hepatocyte Nuclear Factor 1 ; Hepatocyte Nuclear Factor 1-alpha ; Hepatocyte Nuclear Factor 1-beta ; Humans ; Infant ; Kidney Diseases - diagnostic imaging ; Kidney Diseases - genetics ; Kidney Diseases - pathology ; Kidney Failure, Chronic - etiology ; Kidney Failure, Chronic - genetics ; Kidney Glomerulus - diagnostic imaging ; Kidney Glomerulus - pathology ; Male ; Nuclear Proteins ; Pedigree ; Reverse Transcriptase Polymerase Chain Reaction ; Transcription Factors - genetics ; Ultrasonography</subject><ispartof>Pediatric nephrology (Berlin, West), 2002-12, Vol.17 (12), p.1021-1026</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c297t-218dc1f0b82649ece18a83586728df5e55be414a3f7dfe15a5a56480f2638483</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12478351$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mache, Christoph J</creatorcontrib><creatorcontrib>Preisegger, Karl-Heinz</creatorcontrib><creatorcontrib>Kopp, Susanne</creatorcontrib><creatorcontrib>Ratschek, Manfred</creatorcontrib><creatorcontrib>Ring, Ekkehard</creatorcontrib><title>De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><description>Mutations in the gene encoding the transcription factor hepatocyte nuclear factor (HNF)-1 beta are associated with maturity-onset diabetes of the young (type V), non-diabetic renal disease, and occasionally genital malformations in females. Recently, familial hypoplastic glomerulocystic kidney disease (GCKD) has been added to the clinical spectrum of HNF-1 beta gene mutations. Familial hypoplastic GCKD is a rare, dominantly inherited disorder characterized by small kidneys containing glomerular cysts, abnormal pelvicalyceal anatomy, and chronic renal failure. A family with hypoplastic GCKD occurring in the father and the daughter was screened for mutations in the HNF-1 beta gene. The sequence of exon 4 of the HNF-1 beta gene revealed a C insertion at codon 334 resulting in a frameshift mutation (P334fsinsC) in two family members. The P334fsinsC allele co-segregated with hypoplastic GCKD in the family. Oral glucose tolerance testing was normal in the 11-year-old girl. In her 38-year-old father, impaired glucose tolerance was detected. These studies provide further evidence that familial hypoplastic GCKD is associated with HNF-1 beta gene mutations. HNF-1 beta gene mutation screening may prove useful in patients with small cystic kidneys and chronic renal failure, in whom a definite renal diagnosis could otherwise only be established by renal biopsy.</description><subject>Austria</subject><subject>DNA - biosynthesis</subject><subject>DNA - genetics</subject><subject>DNA-Binding Proteins</subject><subject>Female</subject><subject>Frameshift Mutation - genetics</subject><subject>Hepatocyte Nuclear Factor 1</subject><subject>Hepatocyte Nuclear Factor 1-alpha</subject><subject>Hepatocyte Nuclear Factor 1-beta</subject><subject>Humans</subject><subject>Infant</subject><subject>Kidney Diseases - diagnostic imaging</subject><subject>Kidney Diseases - genetics</subject><subject>Kidney Diseases - pathology</subject><subject>Kidney Failure, Chronic - etiology</subject><subject>Kidney Failure, Chronic - genetics</subject><subject>Kidney Glomerulus - diagnostic imaging</subject><subject>Kidney Glomerulus - pathology</subject><subject>Male</subject><subject>Nuclear Proteins</subject><subject>Pedigree</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Transcription Factors - genetics</subject><subject>Ultrasonography</subject><issn>0931-041X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkDFPwzAUhD2AaCn8ABbkic1gO3bsjKhQilTBUgk2y0meiyGJQ5wg5d-T0krohqeT7k5PH0JXjN4yStVdpFSkilDKCc2UJPwEzWmWMEIFe5-h8xg_KaVa6vQMzRgXSieSzdHbA-Am_AS8flkRhnPoLd5BA7geetv70GDfYGdrX3lb4Y-xDW1lY-8LvKtCDd1QhWL881--bGDEpY9gI1ygU2erCJfHu0Db1eN2uSab16fn5f2GFDxTPeFMlwVzNNc8FRkUwLSdHtOp4rp0EqTMQTBhE6dKB0zaSanQ1PE00UInC3RzmG278D1A7E3tYwFVZRsIQzSKq5RrKacgOwSLLsTYgTNt52vbjYZRswdoDgDNBNDsARo-da6P40NeQ_nfONJLfgEXXG2x</recordid><startdate>20021201</startdate><enddate>20021201</enddate><creator>Mache, Christoph J</creator><creator>Preisegger, Karl-Heinz</creator><creator>Kopp, Susanne</creator><creator>Ratschek, Manfred</creator><creator>Ring, Ekkehard</creator><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>20021201</creationdate><title>De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease</title><author>Mache, Christoph J ; Preisegger, Karl-Heinz ; Kopp, Susanne ; Ratschek, Manfred ; Ring, Ekkehard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c297t-218dc1f0b82649ece18a83586728df5e55be414a3f7dfe15a5a56480f2638483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Austria</topic><topic>DNA - biosynthesis</topic><topic>DNA - genetics</topic><topic>DNA-Binding Proteins</topic><topic>Female</topic><topic>Frameshift Mutation - genetics</topic><topic>Hepatocyte Nuclear Factor 1</topic><topic>Hepatocyte Nuclear Factor 1-alpha</topic><topic>Hepatocyte Nuclear Factor 1-beta</topic><topic>Humans</topic><topic>Infant</topic><topic>Kidney Diseases - diagnostic imaging</topic><topic>Kidney Diseases - genetics</topic><topic>Kidney Diseases - pathology</topic><topic>Kidney Failure, Chronic - etiology</topic><topic>Kidney Failure, Chronic - genetics</topic><topic>Kidney Glomerulus - diagnostic imaging</topic><topic>Kidney Glomerulus - pathology</topic><topic>Male</topic><topic>Nuclear Proteins</topic><topic>Pedigree</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Transcription Factors - genetics</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mache, Christoph J</creatorcontrib><creatorcontrib>Preisegger, Karl-Heinz</creatorcontrib><creatorcontrib>Kopp, Susanne</creatorcontrib><creatorcontrib>Ratschek, Manfred</creatorcontrib><creatorcontrib>Ring, Ekkehard</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>Pediatric nephrology (Berlin, West)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mache, Christoph J</au><au>Preisegger, Karl-Heinz</au><au>Kopp, Susanne</au><au>Ratschek, Manfred</au><au>Ring, Ekkehard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease</atitle><jtitle>Pediatric nephrology (Berlin, West)</jtitle><addtitle>Pediatr Nephrol</addtitle><date>2002-12-01</date><risdate>2002</risdate><volume>17</volume><issue>12</issue><spage>1021</spage><epage>1026</epage><pages>1021-1026</pages><issn>0931-041X</issn><abstract>Mutations in the gene encoding the transcription factor hepatocyte nuclear factor (HNF)-1 beta are associated with maturity-onset diabetes of the young (type V), non-diabetic renal disease, and occasionally genital malformations in females. Recently, familial hypoplastic glomerulocystic kidney disease (GCKD) has been added to the clinical spectrum of HNF-1 beta gene mutations. Familial hypoplastic GCKD is a rare, dominantly inherited disorder characterized by small kidneys containing glomerular cysts, abnormal pelvicalyceal anatomy, and chronic renal failure. A family with hypoplastic GCKD occurring in the father and the daughter was screened for mutations in the HNF-1 beta gene. The sequence of exon 4 of the HNF-1 beta gene revealed a C insertion at codon 334 resulting in a frameshift mutation (P334fsinsC) in two family members. The P334fsinsC allele co-segregated with hypoplastic GCKD in the family. Oral glucose tolerance testing was normal in the 11-year-old girl. In her 38-year-old father, impaired glucose tolerance was detected. These studies provide further evidence that familial hypoplastic GCKD is associated with HNF-1 beta gene mutations. HNF-1 beta gene mutation screening may prove useful in patients with small cystic kidneys and chronic renal failure, in whom a definite renal diagnosis could otherwise only be established by renal biopsy.</abstract><cop>Germany</cop><pmid>12478351</pmid><doi>10.1007/s00467-002-0975-2</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0931-041X |
ispartof | Pediatric nephrology (Berlin, West), 2002-12, Vol.17 (12), p.1021-1026 |
issn | 0931-041X |
language | eng |
recordid | cdi_proquest_miscellaneous_72762855 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Austria DNA - biosynthesis DNA - genetics DNA-Binding Proteins Female Frameshift Mutation - genetics Hepatocyte Nuclear Factor 1 Hepatocyte Nuclear Factor 1-alpha Hepatocyte Nuclear Factor 1-beta Humans Infant Kidney Diseases - diagnostic imaging Kidney Diseases - genetics Kidney Diseases - pathology Kidney Failure, Chronic - etiology Kidney Failure, Chronic - genetics Kidney Glomerulus - diagnostic imaging Kidney Glomerulus - pathology Male Nuclear Proteins Pedigree Reverse Transcriptase Polymerase Chain Reaction Transcription Factors - genetics Ultrasonography |
title | De novo HNF-1 beta gene mutation in familial hypoplastic glomerulocystic kidney disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T05%3A08%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=De%20novo%20HNF-1%20beta%20gene%20mutation%20in%20familial%20hypoplastic%20glomerulocystic%20kidney%20disease&rft.jtitle=Pediatric%20nephrology%20(Berlin,%20West)&rft.au=Mache,%20Christoph%20J&rft.date=2002-12-01&rft.volume=17&rft.issue=12&rft.spage=1021&rft.epage=1026&rft.pages=1021-1026&rft.issn=0931-041X&rft_id=info:doi/10.1007/s00467-002-0975-2&rft_dat=%3Cproquest_cross%3E72762855%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=72762855&rft_id=info:pmid/12478351&rfr_iscdi=true |