Literature DB >> 8418655

Osteoporosis-pseudoglioma syndrome.

A De Paepe1, J G Leroy, L Nuytinck, F Meire, J Capoen.   

Abstract

Two patients with osteoporosis pseudoglioma syndrome are described. Both are single children, born to nonconsanguineous, healthy parents. The first patient, a 17-year-old girl, had serious visual impairment since birth. She is severely dwarfed and has major skeletal deformities resulting in inability to walk since age 2 years. The second patient is an 18-year-old girl with unilateral neonatal blindness, short stature and deformities, mainly of pelvis and lower limbs. She has been able to walk with support up to now. The clinical and radiological findings in these 2 patients reflect the clinical variability of the condition. Results of collagen studies in both patients are normal and differentiate this condition clearly from severe osteogenesis imperfecta, which it resembles.

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Year:  1993        PMID: 8418655     DOI: 10.1002/ajmg.1320450110

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


  7 in total

1.  Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.

Authors:  Xiaodong Jiao; Valerio Ventruto; Michael T Trese; Barkur S Shastry; J Fielding Hejtmancik
Journal:  Am J Hum Genet       Date:  2004-09-02       Impact factor: 11.025

2.  Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.

Authors:  Y Gong; M Vikkula; L Boon; J Liu; P Beighton; R Ramesar; L Peltonen; H Somer; T Hirose; B Dallapiccola; A De Paepe; W Swoboda; B Zabel; A Superti-Furga; B Steinmann; H G Brunner; A Jans; R G Boles; W Adkins; M J van den Boogaard; B R Olsen; M L Warman
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

3.  Clinical and molecular findings in osteoporosis-pseudoglioma syndrome.

Authors:  Minrong Ai; Shauna Heeger; Cynthia F Bartels; Deborah K Schelling
Journal:  Am J Hum Genet       Date:  2005-09-27       Impact factor: 11.025

4.  Fractures on bisphosphonates in osteoporosis pseudoglioma syndrome (OPPG): pQCT shows poor bone density and structure.

Authors:  Elizabeth A Streeten; Sheila Ramirez; Myrto Eliades; Sarada Jaimungal; Sruti Chandrasekaran; Ryan Kathleen; D Holmes Morton; Erik G Puffenberger; Rita Herskovitz; Mary B Leonard
Journal:  Bone       Date:  2015-04-16       Impact factor: 4.398

5.  Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects.

Authors:  Craig F Munns; Somayyeh Fahiminiya; Nabin Poudel; Maria Cristina Munteanu; Jacek Majewski; David O Sillence; Jordan P Metcalf; Andrew Biggin; Francis Glorieux; François Fassier; Frank Rauch; Myron E Hinsdale
Journal:  Am J Hum Genet       Date:  2015-05-28       Impact factor: 11.025

6.  Osteoporosis-pseudoglioma syndrome: description of 9 new cases and beneficial response to bisphosphonates.

Authors:  Elizabeth A Streeten; Daniel McBride; Eric Puffenberger; Marc E Hoffman; Toni I Pollin; Patrick Donnelly; Paul Sack; Holmes Morton
Journal:  Bone       Date:  2008-05-07       Impact factor: 4.398

7.  LRP5 and LRP6 are not required for protective antigen-mediated internalization or lethality of anthrax lethal toxin.

Authors:  John J Young; Jennifer L Bromberg-White; Cassandra Zylstra; Joseph T Church; Elissa Boguslawski; James H Resau; Bart O Williams; Nicholas S Duesbery
Journal:  PLoS Pathog       Date:  2007-03       Impact factor: 6.823

  7 in total

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