Literature DB >> 8723082

Sponastrime dysplasia: five new cases and review of nine previously published cases.

L O Langer1, R K Beals, S LaFranchi, C I Scott, J J Sockalosky.   

Abstract

Sponastrime dysplasia (SD) is a dwarfing autosomal recessive short-limb bone dysplasia. The diagnosis is established by a combination of clinical and radiological findings of which the radiological are the more specific. The current diagnostic criteria are ambiguous as demonstrated by the fact that, in our opinion, three of the five patients reported since the original article do not have this condition. Comparison of our five patients and the 9 published patients has led to development of more specific diagnostic criteria. Previously undescribed complications of this condition are subglottic stenosis and tracheo-broncho-malacia, developmental coxa vara, and avascular necrosis of the capital femoral epiphyses.

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Year:  1996        PMID: 8723082     DOI: 10.1002/(SICI)1096-8628(19960503)63:1<20::AID-AJMG7>3.0.CO;2-W

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


  4 in total

1.  Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.

Authors:  Lindsay C Burrage; John J Reynolds; Nissan Vida Baratang; Jennifer B Phillips; Jeremy Wegner; Ashley McFarquhar; Martin R Higgs; Audrey E Christiansen; Denise G Lanza; John R Seavitt; Mahim Jain; Xiaohui Li; David A Parry; Vandana Raman; David Chitayat; Ivan K Chinn; Alison A Bertuch; Lefkothea Karaviti; Alan E Schlesinger; Dawn Earl; Michael Bamshad; Ravi Savarirayan; Harsha Doddapaneni; Donna Muzny; Shalini N Jhangiani; Christine M Eng; Richard A Gibbs; Weimin Bi; Lisa Emrick; Jill A Rosenfeld; John Postlethwait; Monte Westerfield; Mary E Dickinson; Arthur L Beaudet; Emmanuelle Ranza; Celine Huber; Valérie Cormier-Daire; Wei Shen; Rong Mao; Jason D Heaney; Jordan S Orange; Débora Bertola; Guilherme L Yamamoto; Wagner A R Baratela; Merlin G Butler; Asim Ali; Mehdi Adeli; Daniel H Cohn; Deborah Krakow; Andrew P Jackson; Melissa Lees; Amaka C Offiah; Colleen M Carlston; John C Carey; Grant S Stewart; Carlos A Bacino; Philippe M Campeau; Brendan Lee
Journal:  Am J Hum Genet       Date:  2019-02-14       Impact factor: 11.025

2.  Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia.

Authors:  Hae Ryung Chang; Sung Yoon Cho; Jae Hoon Lee; Eunkyung Lee; Jieun Seo; Hye Ran Lee; Denise P Cavalcanti; Outi Mäkitie; Helena Valta; Katta M Girisha; Chung Lee; Kausthubham Neethukrishna; Gandham S Bhavani; Anju Shukla; Sheela Nampoothiri; Shubha R Phadke; Mi Jung Park; Shiro Ikegawa; Zheng Wang; Martin R Higgs; Grant S Stewart; Eunyoung Jung; Myeong-Sok Lee; Jong Hoon Park; Eun A Lee; Hongtae Kim; Kyungjae Myung; Woosung Jeon; Kyoungyeul Lee; Dongsup Kim; Ok-Hwa Kim; Murim Choi; Han-Woong Lee; Yonghwan Kim; Tae-Joon Cho
Journal:  Am J Hum Genet       Date:  2019-02-14       Impact factor: 11.025

Review 3.  SPONASTRIME dysplasia: report of an 11-year-old boy and review of the literature.

Authors:  H A Cooper; J Crowe; M G Butler
Journal:  Am J Med Genet       Date:  2000-05-01

Review 4.  Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts.

Authors:  Karen W Gripp; Caitlyn Johnson; Charles I Scott; Linda Nicholson; Michael Bober; Merlin G Butler; Linda Shaw; Robert J Gorlin
Journal:  Am J Med Genet A       Date:  2008-02-15       Impact factor: 2.802

  4 in total

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