Literature DB >> 21050253

Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets.

Mary D Ruppe1, Patrick G Brosnan, Kit Sing Au, Phong X Tran, Barbara W Dominguez, Hope Northrup.   

Abstract

BACKGROUND: X-linked hypophosphatemic rickets, autosomal dominant hypophosphatemic rickets and autosomal recessive hypophosphatemic rickets make up a group of renal phosphate wasting disorders with common clinical and biochemical characteristics. These three types of rickets are related to mutations in PHEX, FGF23 and dentin matrix protein 1 (DMP1), respectively.
OBJECTIVE: The objective of the study was to evaluate the frequency of mutations that occur in these three genes associated with hypophosphatemic rickets. PATIENTS AND METHODS: In this study, we sequenced these genes in 76 members of 46 kindreds from a large hypophosphatemic rickets cohort.
RESULTS: Forty-two individuals from 27 kindreds were found to have mutations in PHEX; 16 of which were novel. One subject had an FGF23 mutation. No individuals were found to have mutations in DMP1 consistent with the presence of recessive hypophosphatemic rickets.
CONCLUSIONS: Our data highlight the wide spectrum of genetic variation that can be seen in PHEX, FGF23 and DMP1 when screening a large cohort with hypophosphatemic rickets.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21050253      PMCID: PMC3035757          DOI: 10.1111/j.1365-2265.2010.03919.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  38 in total

1.  Discordance for X-linked hypophosphataemic rickets in identical twin girls.

Authors:  Catherine J Owen; Abdul Habeb; Simon H S Pearce; Michael Wright; Shoji Ichikawa; Andrea H Sorenson; Michael J Econs; Tim D Cheetham
Journal:  Horm Res       Date:  2009-03-04

2.  Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.

Authors:  Shoji Ichikawa; Elizabeth A Traxler; Selina A Estwick; Leah R Curry; Michelle L Johnson; Andrea H Sorenson; Erik A Imel; Michael J Econs
Journal:  Bone       Date:  2008-06-18       Impact factor: 4.398

3.  PHEXdb, a locus-specific database for mutations causing X-linked hypophosphatemia.

Authors:  Y Sabbagh; A O Jones; H S Tenenhouse
Journal:  Hum Mutat       Date:  2000       Impact factor: 4.878

4.  Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23.

Authors:  K E White; G Carn; B Lorenz-Depiereux; A Benet-Pages; T M Strom; M J Econs
Journal:  Kidney Int       Date:  2001-12       Impact factor: 10.612

5.  Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23.

Authors: 
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

6.  Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia.

Authors:  T Shimada; S Mizutani; T Muto; T Yoneya; R Hino; S Takeda; Y Takeuchi; T Fujita; S Fukumoto; T Yamashita
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-08       Impact factor: 11.205

7.  PHEX analysis in 118 pedigrees reveals new genetic clues in hypophosphatemic rickets.

Authors:  Céline Gaucher; Odile Walrant-Debray; Thy-Minh Nguyen; Laure Esterle; Michèle Garabédian; Frédéric Jehan
Journal:  Hum Genet       Date:  2009-02-15       Impact factor: 4.132

8.  Incidence and prevalence of nutritional and hereditary rickets in southern Denmark.

Authors:  Signe Sparre Beck-Nielsen; Bendt Brock-Jacobsen; Jeppe Gram; Kim Brixen; Tina Kold Jensen
Journal:  Eur J Endocrinol       Date:  2008-12-18       Impact factor: 6.664

9.  The autosomal dominant hypophosphatemic rickets R176Q mutation in fibroblast growth factor 23 resists proteolytic cleavage and enhances in vivo biological potency.

Authors:  Xiu-Ying Bai; Dengshun Miao; David Goltzman; Andrew C Karaplis
Journal:  J Biol Chem       Date:  2003-01-07       Impact factor: 5.157

10.  Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets.

Authors:  Emily G Farrow; Siobhan I Davis; Leanne M Ward; Lelia J Summers; Judith S Bubbear; Richard Keen; Trevor C B Stamp; Laurence R I Baker; Lynda F Bonewald; Kenneth E White
Journal:  Bone       Date:  2008-10-25       Impact factor: 4.398

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  14 in total

Review 1.  Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding osteopontin: The first digenic SIBLING protein osteopathy?

Authors:  Michael P Whyte; S Deepak Amalnath; William H McAlister; Marc D McKee; Deborah J Veis; Margaret Huskey; Shenghui Duan; Vinieth N Bijanki; Suhas Alur; Steven Mumm
Journal:  Bone       Date:  2019-12-13       Impact factor: 4.398

2.  Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type.

Authors:  Marcos Morey; Lidia Castro-Feijóo; Jesús Barreiro; Paloma Cabanas; Manuel Pombo; Marta Gil; Ignacio Bernabeu; José M Díaz-Grande; Lourdes Rey-Cordo; Gema Ariceta; Itxaso Rica; José Nieto; Ramón Vilalta; Loreto Martorell; Jaime Vila-Cots; Fernando Aleixandre; Ana Fontalba; Leandro Soriano-Guillén; José M García-Sagredo; Sixto García-Miñaur; Berta Rodríguez; Saioa Juaristi; Carmen García-Pardos; Antonio Martínez-Peinado; José M Millán; Ana Medeira; Oana Moldovan; Angeles Fernandez; Lourdes Loidi
Journal:  BMC Med Genet       Date:  2011-09-08       Impact factor: 2.103

3.  Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing.

Authors:  Y Liu; D Ma; F Lv; X Xu; J Wang; W Xia; Y Jiang; O Wang; X Xing; W Yu; J Wang; J Sun; L Song; Y Zhu; H Yang; J Wang; M Li
Journal:  Osteoporos Int       Date:  2017-07-19       Impact factor: 4.507

Review 4.  Insights from genetic disorders of phosphate homeostasis.

Authors:  Marta Christov; Harald Jüppner
Journal:  Semin Nephrol       Date:  2013-03       Impact factor: 5.299

5.  Kbus/Idr, a mutant mouse strain with skeletal abnormalities and hypophosphatemia: identification as an allele of 'Hyp'.

Authors:  Kenji Moriyama; Atsuko Hanai; Kazuyuki Mekada; Atsushi Yoshiki; Katsueki Ogiwara; Atsushi Kimura; Takayuki Takahashi
Journal:  J Biomed Sci       Date:  2011-08-20       Impact factor: 8.410

6.  The developmental trajectory of brain-scalp distance from birth through childhood: implications for functional neuroimaging.

Authors:  Michael S Beauchamp; Michelle R Beurlot; Eswen Fava; Audrey R Nath; Nehal A Parikh; Ziad S Saad; Heather Bortfeld; John S Oghalai
Journal:  PLoS One       Date:  2011-09-21       Impact factor: 3.240

7.  Phenotypes of a family with XLH with a novel PHEX mutation.

Authors:  Akiko Yamamoto; Toshiro Nakamura; Yasuhisa Ohata; Takuo Kubota; Keiichi Ozono
Journal:  Hum Genome Var       Date:  2020-03-31

8.  Identification of two novel mutations in the PHEX gene in Chinese patients with hypophosphatemic rickets/osteomalacia.

Authors:  Hua Yue; Jin-bo Yu; Jin-wei He; Zeng Zhang; Wen-zhen Fu; Hao Zhang; Chun Wang; Wei-wei Hu; Jie-mei Gu; Yun-qiu Hu; Miao Li; Yu-juan Liu; Zhen-Lin Zhang
Journal:  PLoS One       Date:  2014-05-16       Impact factor: 3.240

9.  Milk Products in the Treatment of Hypophosphatemic Rickets: A Pilot Study.

Authors:  Cecilie Siggaard Jørgensen; Vibe Morgana Lund Poulsen; Mads Sandahl; Line Underbjerg; Simon Bang Kristensen; Isabelle Piec; Signe Sparre Beck-Nielsen; Lars Rejnmark; Niels Holtum Birkebæk
Journal:  Int J Endocrinol Metab       Date:  2019-10-06

10.  A novel c.2179T>C mutation blocked the intracellular transport of PHEX protein and caused X-linked hypophosphatemic rickets in a Chinese family.

Authors:  Baowei Li; Xiong Wang; Xiaodan Hao; Yanran Liu; Yin Wang; Chan Shan; Xiang Ao; Ying Liu; HongChu Bao; Peifeng Li
Journal:  Mol Genet Genomic Med       Date:  2020-06-08       Impact factor: 2.183

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