Literature DB >> 9056558

New progeroid disorder.

M Penttinen1, K M Niemi, H Vinkka-Puhakka, R Johansson, P Aula.   

Abstract

We report on a 10-year-old Caucasian male with a prematurely aged appearance, delayed bone maturation and dental development, pronounced acro-osteolysis with brachydactyly, and distinctive cutaneous findings including hard, confluent skin lesions with some clinical and histologic resemblance to those of juvenile hyaline fibromatosis (JHF). He also had hyperopia, sensorineural hearing loss, and elevated TSH. Linear growth and intellectual functions were normal. We believe that this patient represents a new progeroid disorder.

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Year:  1997        PMID: 9056558

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome.

Authors:  Jennifer J Johnston; Monica Y Sanchez-Contreras; Kim M Keppler-Noreuil; Julie Sapp; Molly Crenshaw; NiCole A Finch; Valerie Cormier-Daire; Rosa Rademakers; Virginia P Sybert; Leslie G Biesecker
Journal:  Am J Hum Genet       Date:  2015-08-13       Impact factor: 11.025

2.  A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome.

Authors:  Cecilie Bredrup; Tomasz Stokowy; Julie McGaughran; Samuel Lee; Dipak Sapkota; Ileana Cristea; Linda Xu; Kåre Steinar Tveit; Gunnar Høvding; Vidar Martin Steen; Eyvind Rødahl; Ove Bruland; Gunnar Houge
Journal:  Eur J Hum Genet       Date:  2018-12-20       Impact factor: 4.246

Review 3.  Acro-osteolysis.

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

Review 4.  PDGF receptor mutations in human diseases.

Authors:  Emilie Guérit; Florence Arts; Guillaume Dachy; Boutaina Boulouadnine; Jean-Baptiste Demoulin
Journal:  Cell Mol Life Sci       Date:  2021-01-15       Impact factor: 9.261

  4 in total

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