Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies

被引：82

作者：

Koenig, Jens ^{[1
]}

Kranz, Birgitta ^{[1
]}

Koenig, Sabine ^{[1
]}

Schlingmann, Karl Peter ^{[1
]}

Titieni, Andrea ^{[1
]}

Toenshoff, Burkhard ^{[1
]}

Habbig, Sandra ^{[1
]}

Pape, Lars ^{[1
]}

Haeffner, Karsten ^{[1
]}

Hansen, Matthias ^{[1
]}

Buescher, Anja ^{[1
]}

Bald, Martin ^{[1
]}

Billing, Heiko ^{[1
]}

Schild, Raphael ^{[1
]}

Walden, Ulrike ^{[1
]}

Hampel, Tobias ^{[1
]}

Staude, Hagen ^{[1
]}

Riedl, Magdalena ^{[1
]}

Gretz, Norbert ^{[1
]}

Lablans, Martin ^{[1
]}

Bergmann, Carsten ^{[1
]}

Hildebrandt, Friedhelm ^{[1
]}

Omran, Heymut ^{[1
]}

Konrad, Martin ^{[1
]}

机构：

[1] Univ Childrens Hosp Munster, Dept Gen Pediat, Albert Schweitzer Campus 1, D-48149 Munster, Germany

来源：

CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2017年 / 12卷 / 12期

关键词：

FAMILIAL JUVENILE NEPHRONOPHTHISIS; CYSTIC KIDNEY-DISEASE; SENIOR-LOKEN SYNDROME; ADOLESCENT NEPHRONOPHTHISIS; JOUBERT-SYNDROME; DOMAIN PROTEIN; RENAL-FAILURE; MUTATIONS; GENE; NPHP3;

D O I：

10.2215/CJN.01280217

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Background and objectives Genetic heterogeneity and phenotypic variability are major challenges in familial nephronophthisis and related ciliopathies. To date, mutations in 20 different genes (NPHP1 to -20) have been identified causing either isolated kidney disease or complex multiorgan disorders. In this study, we provide a comprehensive and detailed characterization of 152 childrenwith a special focus on extrarenal organ involvement and the long-term development of ESRD. Design, setting, participants, & measurements We established an online-based registry (www.nephreg.de) to assess the clinical course of patients with nephronophthisis and related ciliopathies on a yearly base. Cross-sectional and longitudinal data were collected. Mean observation time was 7.5 +/- 6.1 years. Results In total, 51% of the children presented with isolated nephronophthisis, whereas the other 49% exhibited related ciliopathies. Monogenetic defects were identified in 97 of 152 patients, 89 affecting NPHP genes. Eight patients carriedmutations inother genes related to cystic kidney diseases. AhomozygousNPHP1deletionwas, by far, themost frequentgenetic defect (n= 60). We observedahighprevalence of extrarenalmanifestations (23%[14of 60] for the NPHP1 group and 66% [61 of 92] for children without NPHP1). A homozygous NPHP1 deletion not only led to juvenile nephronophthisis but also was able to present as a predominantly neurologic phenotype. However, irrespective of the initial clinical presentation, the kidney function of all patients carrying NPHP1 mutations declined rapidly between the ages of 8 and 16 years, with ESRD at a mean age of 11.4 +/- 2.4 years. In contrast within the non-NPHP1 group, there was no uniform pattern regarding the development of ESRD comprising patients with early onset and others preserving normal kidney function until adulthood. Conclusions Mutations in NPHP genes cause a wide range of ciliopathies with multiorgan involvement and different clinical outcomes.

引用

页码：1974 / 1983

页数：10

共 46 条

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