Literature DB >> 17506093

Oculo-auriculo-vertebral spectrum: associated anomalies, functional deficits and possible developmental risk factors.

Kerstin Strömland1, Marilyn Miller, Lotta Sjögreen, Maria Johansson, Britt-Marie Ekman Joelsson, Eva Billstedt, Christopher Gillberg, Susanna Danielsson, Catharina Jacobsson, Jan Andersson-Norinder, Gösta Granström.   

Abstract

Swedish patients with the oculo-auriculo-vertebral (OAV) spectrum participated in a prospective multidisciplinary investigation. The aims of the study were to describe their systemic and functional defects, especially autism spectrum disorders, and to search for possible etiologic risk factors. Available medical records were studied and the mothers answered a questionnaire on history of prenatal events. A clinical examination evaluating systemic findings, vision, hearing, speech, oral and swallowing function, and neuropsychiatric function, especially autism, was made. Eighteen patients, (11 males, 7 females) aged 8 months to 17 years with OAV were studied. Most frequent systemic malformations included, ear abnormalities (100%), ocular malformations (72%), vertebral deformities (67%), cerebral anomalies (50%), and congenital heart defects (33%). Functional defects consisted of hearing impairment (83%), visual impairment (28%), both visual and hearing impairment (28%), difficulties in feeding/eating (50%), speech (53%), mental retardation (39%), and severe autistic symptoms (11%). Three children were born following assisted fertilization (two intracytoplasmatic sperm injection, one in vitro fertilization), two mothers reported early bleedings, and six (33%) mothers had smoked during pregnancy.

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Year:  2007        PMID: 17506093     DOI: 10.1002/ajmg.a.31769

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  27 in total

1.  [Analysis of an ophthalmic pathology cohort of human fetal eyes with regard to interesting findings].

Authors:  M C Herwig; A M Müller; F G Holz; K U Loeffler
Journal:  Ophthalmologe       Date:  2010-11       Impact factor: 1.059

2.  Ophthalmic features and management outcomes of 30 children having Goldenhar syndrome.

Authors:  Manpreet Singh; Manpreet Kaur; Aditi Mehta Grewal; Sonam Yangzes; Deepti Yadav; Zoramthara Zadeng; Pankaj Gupta
Journal:  Int Ophthalmol       Date:  2019-11-23       Impact factor: 2.031

3.  Psychosocial outcomes in children with hemifacial microsomia.

Authors:  Lynette M Dufton; Matthew L Speltz; Judith P Kelly; Brian Leroux; Brent R Collett; Martha M Werler
Journal:  J Pediatr Psychol       Date:  2011-02-23

Review 4.  Goldenhar syndrome: current perspectives.

Authors:  Katarzyna Bogusiak; Aleksandra Puch; Piotr Arkuszewski
Journal:  World J Pediatr       Date:  2017-06-15       Impact factor: 2.764

Review 5.  Craniofacial malformations and the orthodontist.

Authors:  A Akram; M M McKnight; H Bellardie; V Beale; R D Evans
Journal:  Br Dent J       Date:  2015-02-16       Impact factor: 1.626

6.  Health-related quality of life in children with hemifacial microsomia: parent and child perspectives.

Authors:  Mary A Khetani; Brent R Collett; Matthew L Speltz; Martha M Werler
Journal:  J Dev Behav Pediatr       Date:  2013 Nov-Dec       Impact factor: 2.225

Review 7.  Hemifacial microsomia: skeletal abnormalities evaluation using CBCT (case report).

Authors:  Sergey Lvovich Kabak; Nina Alexandrovna Savrasova; Valentina Vladimirovna Zatochnaya; Yuliya Michailovna Melnichenko
Journal:  J Radiol Case Rep       Date:  2019-11-30

8.  Sleep outcomes in children with hemifacial microsomia and controls: a follow-up study.

Authors:  Yona K Cloonan; Yemiserach Kifle; Scott Davis; Matthew L Speltz; Martha M Werler; Jacqueline R Starr
Journal:  Pediatrics       Date:  2009-07-27       Impact factor: 7.124

9.  Speech, Language, and Communication Skills of Adolescents With Craniofacial Microsomia.

Authors:  Brent R Collett; Kathy Chapman; Erin R Wallace; Sara L Kinter; Carrie L Heike; Matthew L Speltz; Martha Werler
Journal:  Am J Speech Lang Pathol       Date:  2019-10-03       Impact factor: 2.408

10.  Craniofacial abnormalities among patients with Edwards Syndrome.

Authors:  Rafael Fabiano M Rosa; Rosana Cardoso M Rosa; Marina Boff Lorenzen; Paulo Ricardo G Zen; Carla Graziadio; Giorgio Adriano Paskulin
Journal:  Rev Paul Pediatr       Date:  2013-09
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