Literature DB >> 25007883

A new acro-osteolysis syndrome caused by duplications including PTHLH.

Mary J Gray1, Margriet van Kogelenberg1, Rachel Beddow2, Tim Morgan1, Paul Wordsworth3, Deborah J Shears4, Stephen P Robertson1, Jane A Hurst5.   

Abstract

Parathyroid hormone-like hormone (PTHLH, MIM 168470) is a humoral factor, structurally and functionally related to parathyroid hormone, which mediates multiple effects on chondrocyte, osteoblast and osteoclast function. Mutations and copy number imbalances of the PTHLH locus and in the gene encoding its receptor, PTHR1, result in a variety of skeletal dysplasias including brachydactyly type E, Eiken syndrome, Jansen metaphyseal chondrodysplasia and Blomstrand type chondrodysplasia. Here we describe three individuals with duplications of the PTHLH locus, including two who are mosaic for these imbalances, leading to a hitherto unrecognized syndrome characterized by acro-osteolysis, cortical irregularity of long bones and metadiaphyseal enchondromata.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25007883     DOI: 10.1038/jhg.2014.58

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  10 in total

1.  Metaphyseal chondrodysplasia, type Jansen.

Authors:  K Kozlowski; J B Campbell; M E Azouz; P Sprague
Journal:  Australas Radiol       Date:  1999-11

2.  Multiplex Ligation-dependent Probe Amplification (MLPA®) for the detection of copy number variation in genomic sequences.

Authors:  Petra G C Eijk-Van Os; Jan P Schouten
Journal:  Methods Mol Biol       Date:  2011

3.  Deletion and point mutations of PTHLH cause brachydactyly type E.

Authors:  Eva Klopocki; Bianca P Hennig; Katarina Dathe; Randi Koll; Thomy de Ravel; Emiel Baten; Eveline Blom; Yves Gillerot; Johannes F W Weigel; Gabriele Krüger; Olaf Hiort; Petra Seemann; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2010-02-18       Impact factor: 11.025

4.  Rab15 effector protein: a novel protein for receptor recycling from the endocytic recycling compartment.

Authors:  David J Strick; Lisa A Elferink
Journal:  Mol Biol Cell       Date:  2005-09-29       Impact factor: 4.138

Review 5.  PTHrP and skeletal development.

Authors:  Henry M Kronenberg
Journal:  Ann N Y Acad Sci       Date:  2006-04       Impact factor: 5.691

6.  Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss.

Authors:  Michael A Simpson; Melita D Irving; Esra Asilmaz; Mary J Gray; Dimitra Dafou; Frances V Elmslie; Sahar Mansour; Sue E Holder; Caroline E Brain; Barbara K Burton; Katherine H Kim; Richard M Pauli; Salim Aftimos; Helen Stewart; Chong Ae Kim; Muriel Holder-Espinasse; Stephen P Robertson; William M Drake; Richard C Trembath
Journal:  Nat Genet       Date:  2011-03-06       Impact factor: 38.330

7.  Symmetrical enchondromatosis is associated with duplication of 12p11.23 to 12p11.22 including PTHLH.

Authors:  Morag Collinson; Samantha J Leonard; Jocelyn Charlton; John A Crolla; Caroline Silve; Christine M Hall; Colin Oglivie; Margaret A James; Sarah F Smithson
Journal:  Am J Med Genet A       Date:  2010-12       Impact factor: 2.802

8.  A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E.

Authors:  Philipp G Maass; Jutta Wirth; Atakan Aydin; Andreas Rump; Sigmar Stricker; Sigrid Tinschert; Miguel Otero; Kaneyuki Tsuchimochi; Mary B Goldring; Friedrich C Luft; Sylvia Bähring
Journal:  Hum Mol Genet       Date:  2009-12-16       Impact factor: 6.150

9.  The Cul3/Klhdc5 E3 ligase regulates p60/katanin and is required for normal mitosis in mammalian cells.

Authors:  Cristina M Cummings; Cornelia A Bentley; Sarah A Perdue; Peter W Baas; Jeffrey D Singer
Journal:  J Biol Chem       Date:  2009-03-04       Impact factor: 5.157

10.  The Jansen type of metaphyseal chondrodysplasia: confirmation of dominant inheritance and review of radiographic manifestations in the newborn and adult.

Authors:  J Charrow; A K Poznanski
Journal:  Am J Med Genet       Date:  1984-06
  10 in total
  5 in total

Review 1.  Acro-osteolysis.

Authors:  Anna Botou; Athanasios Bangeas; Ioannis Alexiou; Lazaros I Sakkas
Journal:  Clin Rheumatol       Date:  2016-10-29       Impact factor: 2.980

2.  Duplication of PTHLH causes osteochondroplasia with a combined brachydactyly type E/A1 phenotype with disturbed bone maturation and rhizomelia.

Authors:  Ricarda Flöttmann; Anna Sowinska-Seidler; Julie Lavie; Jean-François Chateil; Didier Lacombe; Stefan Mundlos; Denise Horn; Malte Spielmann
Journal:  Eur J Hum Genet       Date:  2016-01-06       Impact factor: 4.246

3.  What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis.

Authors:  Arrate Pereda; Intza Garin; Guiomar Perez de Nanclares
Journal:  BMC Med Genet       Date:  2018-03-02       Impact factor: 2.103

4.  Is an association of acro-osteolysis, bone fragility, and enchondromatosis a newfound disease caused by an amplification of PTHLH? A case report.

Authors:  Stéphane Echaubard; Céline Pebrel-Richard; Aurélie Chausset; Jean-Louis Kemeny; Etienne Merlin; Fanny Laffargue
Journal:  Pediatr Rheumatol Online J       Date:  2022-07-30       Impact factor: 3.413

Review 5.  Lost bones: differential diagnosis of acro-osteolysis seen by the pediatric rheumatologist.

Authors:  Elizaveta Limenis; Jennifer Stimec; Peter Kannu; Ronald M Laxer
Journal:  Pediatr Rheumatol Online J       Date:  2021-07-14       Impact factor: 3.054

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.