1997
DOI: 10.1111/j.1469-8749.1997.tb07422.x
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Prevalence and type of cerebral palsy in a British ethnic community: the role of consanguinity

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Cited by 50 publications
(25 citation statements)
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“…While most of the conditions so far mentioned are recognised as single-gene autosomal recessive disorders, several other disorders which may or may not have a genetic component are also seen at increased prevalence in UK Pakistani children. For example, except for some rare ataxic syndromes, cerebral palsy is not thought of as having a genetic basis, but a 1997 report from Bradford described both a significantly increased prevalence in Asian children and a positive family history in more than one quarter of these children [43] . Similar findings have been made in Saudi Arabia [44] and Turkey [45] , and Mitchell and Bundey [46] reported on 18 Pakistani patients from 7 families in the English West Midlands, where there seemed to be a familial pattern of cerebral palsy, with a region of homozygosity identified at chromosome 2q24-q25 in 3 of these families [47] .…”
Section: Increased Numbers Of Conditions Not Confirmed As Autosomal Rmentioning
confidence: 99%
“…While most of the conditions so far mentioned are recognised as single-gene autosomal recessive disorders, several other disorders which may or may not have a genetic component are also seen at increased prevalence in UK Pakistani children. For example, except for some rare ataxic syndromes, cerebral palsy is not thought of as having a genetic basis, but a 1997 report from Bradford described both a significantly increased prevalence in Asian children and a positive family history in more than one quarter of these children [43] . Similar findings have been made in Saudi Arabia [44] and Turkey [45] , and Mitchell and Bundey [46] reported on 18 Pakistani patients from 7 families in the English West Midlands, where there seemed to be a familial pattern of cerebral palsy, with a region of homozygosity identified at chromosome 2q24-q25 in 3 of these families [47] .…”
Section: Increased Numbers Of Conditions Not Confirmed As Autosomal Rmentioning
confidence: 99%
“…Clinicians and researchers categorize cerebral palsy into spastic (60–70%), dyskinetic or athetoid (20–30%), and ataxic types (5–10%), in accordance with the muscle tone and format of the movement disorder (predominant abnormality) arising from brain damage2 ) . Since children with cerebral palsy have diverse reflex, muscle tone, and movement patterns3 ) , there is need for the evaluation of the quality of motor activities and method of executing these activities.…”
Section: Introductionmentioning
confidence: 99%
“…It was also the second Canadian-based study to accomplish this. All previous studies were based on information gathered from cerebral palsy registries or exhaustive record searches (Al-Rajeh et al, 1991;Nottidge and Okogbo, 1991;Grether et al, 1992;Hagberg et al, 1993;Murphy et al, 1993;Krageloh-Mann et al, 1994;MacGillivray and Campbell, 1995;Meberg and Broch, 1995;Hagberg et al, 1996;Pharoah et al, 1996;Sinha et al, 1997;Topp et al, 1997;Kavcic and Perat, 1998;Pharoah et al, 1998;Robertson et al, 1998;Bottos et al, 1999;Sciberras and Spencer, 1999;Colver et al, 2000;Stanley et al, 2000;Surveillance of Cerebral Palsy in Europe, 2000;Hagberg et al, 2001;Parkes et al, 2001;Topp et al, 2001;Suzuki and Ito, 2002;and Cans et al, 2004).…”
Section: Population-based Record Linkagementioning
confidence: 99%
“…Pharoah et al (1996) agreed that the prevalenee of eerebral palsy among ehildren weighing greater than 2500 grams has remained steady at about 1. In a study conducted by Sinha, Corry, Subesinghe, Wild and Levene (1997), the prevalenee of eerebral palsy was measured in an Asian community that was predominantly Pakistani Muslim, in the northeast of England. Cases of eerebral palsy were identified using the Yorkshire Regional Cerebral Palsy Register.…”
Section: The Epidemiology Of Cerebral Palsymentioning
confidence: 99%
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