Literature DB >> 2260563

Cerebral palsy in multiple births in Western Australia: genetic aspects.

B Petterson1, F Stanley, D Henderson.   

Abstract

A study of cerebral palsy in multiple births was undertaken to test genetic involvement and assess the impact of the special conditions of pregnancy and parturition in these cases. Complete ascertainment of cerebral palsy in multiple gestations that occurred in Western Australia between 1956 and 1985 was obtained from the Western Australian Cerebral Palsy Register. There were 74 twins and 5 triplets. Data on sex, birth order, motor handicap, outcome in co-twins and triplets, zygosity, and pedigree information was obtained from the Register, hospital records, and, where possible, by interview of the parent(s) of the propositi. There was a significantly higher (P = 0.0026) concordance rate in MZ than in DZ twin pairs. However, pedigree studies showed no other relatives with a motor handicap similar to that of the propositi. This is consistent with a multifactorial cause in at least some of the cases. The sex ratio of affected twins was found to be 2.1 compared to 1.3 for singletons and all 5 affected triplets were boys. The trend of increasing sex ratio with increasing plurality was significant at the 1% level.

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Year:  1990        PMID: 2260563     DOI: 10.1002/ajmg.1320370311

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


  11 in total

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2.  Identifying multiple gestation groups using state-level birth and fetal death certificate data.

Authors:  Jane Lazar; Milton Kotelchuck; Angela Nannini; Mary Barger
Journal:  Matern Child Health J       Date:  2005-11-19

3.  Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability.

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4.  Rare copy number variation in cerebral palsy.

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Journal:  Eur J Hum Genet       Date:  2013-05-22       Impact factor: 4.246

5.  Twins, triplets, and cerebral palsy in births in Western Australia in the 1980s.

Authors:  B Petterson; K B Nelson; L Watson; F Stanley
Journal:  BMJ       Date:  1993-11-13

6.  A review on automatic analysis of human embryo microscope images.

Authors:  E Santos Filho; J A Noble; D Wells
Journal:  Open Biomed Eng J       Date:  2010-10-11

7.  Targeted resequencing identifies genes with recurrent variation in cerebral palsy.

Authors:  C L van Eyk; M A Corbett; M S B Frank; D L Webber; M Newman; J G Berry; K Harper; B P Haines; G McMichael; J A Woenig; A H MacLennan; J Gecz
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8.  Effect of neonatal neuronal intensive care unit on neonatal encephalopathy.

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9.  Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

Authors:  Sheng Chih Jin; Sara A Lewis; Somayeh Bakhtiari; Xue Zeng; Michael C Sierant; Sheetal Shetty; Sandra M Nordlie; Aureliane Elie; Mark A Corbett; Bethany Y Norton; Clare L van Eyk; Shozeb Haider; Brandon S Guida; Helen Magee; James Liu; Stephen Pastore; John B Vincent; Janice Brunstrom-Hernandez; Antigone Papavasileiou; Michael C Fahey; Jesia G Berry; Kelly Harper; Chongchen Zhou; Junhui Zhang; Boyang Li; Hongyu Zhao; Jennifer Heim; Dani L Webber; Mahalia S B Frank; Lei Xia; Yiran Xu; Dengna Zhu; Bohao Zhang; Amar H Sheth; James R Knight; Christopher Castaldi; Irina R Tikhonova; Francesc López-Giráldez; Boris Keren; Sandra Whalen; Julien Buratti; Diane Doummar; Megan Cho; Kyle Retterer; Francisca Millan; Yangong Wang; Jeff L Waugh; Lance Rodan; Julie S Cohen; Ali Fatemi; Angela E Lin; John P Phillips; Timothy Feyma; Suzanna C MacLennan; Spencer Vaughan; Kylie E Crompton; Susan M Reid; Dinah S Reddihough; Qing Shang; Chao Gao; Iona Novak; Nadia Badawi; Yana A Wilson; Sarah J McIntyre; Shrikant M Mane; Xiaoyang Wang; David J Amor; Daniela C Zarnescu; Qiongshi Lu; Qinghe Xing; Changlian Zhu; Kaya Bilguvar; Sergio Padilla-Lopez; Richard P Lifton; Jozef Gecz; Alastair H MacLennan; Michael C Kruer
Journal:  Nat Genet       Date:  2020-09-28       Impact factor: 41.307

10.  A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency.

Authors:  Muhammad Jameel; Joakim Klar; Muhammad Tariq; Abubakar Moawia; Naveed Altaf Malik; Syeda Seema Waseem; Uzma Abdullah; Tahir Naeem Khan; Raili Raininko; Shahid Mahmood Baig; Niklas Dahl
Journal:  BMC Med Genet       Date:  2014-12-14       Impact factor: 2.103

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