Literature DB >> 28808977

Skeletal Dysplasias: What Every Bone Health Clinician Needs to Know.

Sarah M Nikkel1.   

Abstract

PURPOSE OF REVIEW: This review highlights how skeletal dysplasias are diagnosed and how our understanding of some of these conditions has now translated to treatment options. RECENT
FINDINGS: The use of multigene panels, using next-generation sequence technology, has improved our ability to quickly identify the genetic etiology, which can impact management. There are successes with the use of growth hormone in individuals with SHOX deficiencies, asfotase alfa in hypophosphatasia, and some promising data for c-type natriuretic peptide for those with achondroplasia. One needs to consider that a patient with short stature has a skeletal dysplasia as options for management may be available.

Entities:  

Keywords:  C-type natriuretic peptide; Enzyme replacement therapy; Gene panels; Radiographs; Skeletal dysplasias

Mesh:

Substances:

Year:  2017        PMID: 28808977     DOI: 10.1007/s11914-017-0392-x

Source DB:  PubMed          Journal:  Curr Osteoporos Rep        ISSN: 1544-1873            Impact factor:   5.096


  18 in total

1.  Hearing loss in skeletal dysplasia patients.

Authors:  David Tunkel; Yewande Alade; Richard Kerbavaz; Beth Smith; Danielle Rose-Hardison; Julie Hoover-Fong
Journal:  Am J Med Genet A       Date:  2012-05-24       Impact factor: 2.802

2.  [International nomenclature of constitutional diseases of bones].

Authors: 
Journal:  Ann Radiol (Paris)       Date:  1970

3.  Health supervision for children with achondroplasia.

Authors:  Tracy L Trotter; Judith G Hall
Journal:  Pediatrics       Date:  2005-09       Impact factor: 7.124

4.  Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness.

Authors:  Katerina Hirschfeldova; Martina Florianova; Vera Kebrdlova; Marketa Urbanova; Jitka Stekrova
Journal:  J Hum Genet       Date:  2016-10-06       Impact factor: 3.172

Review 5.  Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment.

Authors:  Michael P Whyte
Journal:  Nat Rev Endocrinol       Date:  2016-02-19       Impact factor: 43.330

Review 6.  Bisphosphonate therapy for osteogenesis imperfecta.

Authors:  Kerry Dwan; Carrie A Phillipi; Robert D Steiner; Donald Basel
Journal:  Cochrane Database Syst Rev       Date:  2016-10-19

7.  Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway.

Authors:  Akihiro Yasoda; Yasato Komatsu; Hideki Chusho; Takashi Miyazawa; Ami Ozasa; Masako Miura; Tatsuya Kurihara; Tomohiro Rogi; Shoji Tanaka; Michio Suda; Naohisa Tamura; Yoshihiro Ogawa; Kazuwa Nakao
Journal:  Nat Med       Date:  2003-12-14       Impact factor: 53.440

8.  Neutral endopeptidase-resistant C-type natriuretic peptide variant represents a new therapeutic approach for treatment of fibroblast growth factor receptor 3-related dwarfism.

Authors:  Daniel J Wendt; Melita Dvorak-Ewell; Sherry Bullens; Florence Lorget; Sean M Bell; Jeff Peng; Sianna Castillo; Mika Aoyagi-Scharber; Charles A O'Neill; Pavel Krejci; William R Wilcox; David L Rimoin; Stuart Bunting
Journal:  J Pharmacol Exp Ther       Date:  2015-02-03       Impact factor: 4.030

9.  Enzyme replacement therapy for treating mucopolysaccharidosis type IVA (Morquio A syndrome): effect and limitations.

Authors:  Shunji Tomatsu; Kazuki Sawamoto; Tsutomu Shimada; Michael B Bober; Francyne Kubaski; Eriko Yasuda; Robert W Mason; Shaukat Khan; Carlos J Alméciga-Díaz; Luis A Barrera; William G Mackenzie; Tadao Orii
Journal:  Expert Opin Orphan Drugs       Date:  2015-10-29       Impact factor: 0.694

10.  Evaluation of the therapeutic potential of a CNP analog in a Fgfr3 mouse model recapitulating achondroplasia.

Authors:  Florence Lorget; Nabil Kaci; Jeff Peng; Catherine Benoist-Lasselin; Emilie Mugniery; Todd Oppeneer; Dan J Wendt; Sean M Bell; Sherry Bullens; Stuart Bunting; Laurie S Tsuruda; Charles A O'Neill; Federico Di Rocco; Arnold Munnich; Laurence Legeai-Mallet
Journal:  Am J Hum Genet       Date:  2012-11-29       Impact factor: 11.025

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  5 in total

1.  Changes in skeletal dysplasia nosology.

Authors:  Maria Claudia Jurcă; Sânziana Iulia Jurcă; Filip Mirodot; Bogdan Bercea; Emilia Maria Severin; Marius Bembea; Alexandru Daniel Jurcă
Journal:  Rom J Morphol Embryol       Date:  2021 Jul-Sep       Impact factor: 0.833

2.  Not all the bowlegs is rickets! (a case report).

Authors:  Keta Vagha; Patel Zeeshan Jameel; Jayant Vagha; Ashish Varma; Siddhartha Murhekar; Parameshwar Reddy; Spandana Madirala
Journal:  Pan Afr Med J       Date:  2022-06-29

3.  Revisiting the Population Genetics of Human Height.

Authors:  Peter Rotwein
Journal:  J Endocr Soc       Date:  2020-03-05

4.  Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.

Authors:  Ting-Yu Chang; I-Fang Chung; Wan-Ju Wu; Shun-Ping Chang; Wen-Hsiang Lin; Norman A Ginsberg; Gwo-Chin Ma; Ming Chen
Journal:  Diagnostics (Basel)       Date:  2020-05-07

Review 5.  The evolving therapeutic landscape of genetic skeletal disorders.

Authors:  Ataf Hussain Sabir; Trevor Cole
Journal:  Orphanet J Rare Dis       Date:  2019-12-30       Impact factor: 4.123

  5 in total

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