Literature DB >> 7200838

Three distinct types of X-linked arthrogryposis seen in 6 families.

J G Hall, S D Reed, C I Scott, J G Rogers, K L Jones, A Camarano.   

Abstract

Six families with arthrogryposis (congenital contractures) inherited in an X-linked recessive manner are reported. Family histories from a study of over 350 patients with congenital contractures of the joints (arthrogryposis) were reviewed and of these, three probands had family histories consistent with X-linked recessive inheritance. Three other families were recognized through correspondence. Three forms of X-linked recessively inherited arthrogryposis are described: (1) Severe lethal X-linked arthrogryposis with severe contractures scoliosis deformities, hypotonia, and death due to respiratory insufficiency within 3 months of birth (1 family); (2) Moderately severe X-linked arthrogryposis with severe contractures, ptosis, microphallus, cryptorchidism, inguinal hernias, and normal intelligence (2 families); and (3) Resolving X-linked arthrogryposis with mild to moderate contractures at birth which improve dramatically with time (2 families and 1 sporadic case).

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Mesh:

Year:  1982        PMID: 7200838     DOI: 10.1111/j.1399-0004.1982.tb00742.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  5 in total

1.  Lethal Pena-Shokeir 1 syndrome in three male siblings.

Authors:  T Gyr; M Katz; H J Altermatt; S Braga; P Duerig; C Koenig; H Schneider
Journal:  Arch Gynecol Obstet       Date:  1992       Impact factor: 2.344

2.  Multiple pterygium syndrome type Escobar in two brothers. Follow-up data from childhood to adulthood.

Authors:  J P Fryns; P Volcke; H van den Berghe
Journal:  Eur J Pediatr       Date:  1988-06       Impact factor: 3.183

3.  ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

Authors:  Hiromi Hirata; Indrajit Nanda; Anne van Riesen; Gai McMichael; Hao Hu; Melanie Hambrock; Marie-Amélie Papon; Ute Fischer; Sylviane Marouillat; Can Ding; Servane Alirol; Melanie Bienek; Sabine Preisler-Adams; Astrid Grimme; Dominik Seelow; Richard Webster; Eric Haan; Alastair MacLennan; Werner Stenzel; Tzu Ying Yap; Alison Gardner; Lam Son Nguyen; Marie Shaw; Nicolas Lebrun; Stefan A Haas; Wolfram Kress; Thomas Haaf; Elke Schellenberger; Jamel Chelly; Géraldine Viot; Lisa G Shaffer; Jill A Rosenfeld; Nancy Kramer; Rena Falk; Dima El-Khechen; Luis F Escobar; Raoul Hennekam; Peter Wieacker; Christoph Hübner; Hans-Hilger Ropers; Jozef Gecz; Markus Schuelke; Frédéric Laumonnier; Vera M Kalscheuer
Journal:  Am J Hum Genet       Date:  2013-04-25       Impact factor: 11.025

4.  Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.

Authors:  Z Borochowitz; B Glick; S Blazer
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

Review 5.  A family with severe X-linked arthrogryposis.

Authors:  R C Hennekam; P G Barth; W Van Lookeren Campagne; M De Visser; K P Dingemans
Journal:  Eur J Pediatr       Date:  1991-07       Impact factor: 3.183

  5 in total

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