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Identical syndromes of cerebral palsy in the same family.

作者信息

Gustavson K H, Hagberg B, Sanner G

出版信息

Acta Paediatr Scand. 1969 Jul;58(4):330-40. doi: 10.1111/j.1651-2227.1969.tb04729.x.

DOI:10.1111/j.1651-2227.1969.tb04729.x

PMID:5824822

Abstract

摘要

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相似文献

Identical syndromes of cerebral palsy in the same family.

Acta Paediatr Scand. 1969 Jul;58(4):330-40. doi: 10.1111/j.1651-2227.1969.tb04729.x.

[Causes of cerebral palsy. 4. The CP-syndrome with genetic background].

Lakartidningen. 1969 Apr 23;66(17):1773-9.

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Clin Orthop Relat Res. 1974 Mar-Apr(99):2-11. doi: 10.1097/00003086-197403000-00001.

Recurrence risks in families of children with symmetrical spasticity.

Dev Med Child Neurol. 1977 Apr;19(2):179-91. doi: 10.1111/j.1469-8749.1977.tb07968.x.

Consideration of genetic factors in cerebral palsy.

Dev Med Child Neurol. 1985 Jun;27(3):325-30. doi: 10.1111/j.1469-8749.1985.tb04543.x.

Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy.

Clin Genet. 1997 Jan;51(1):7-14. doi: 10.1111/j.1399-0004.1997.tb02406.x.

Schizencephaly: case report of familial incidence.

Pediatr Neurol. 1992 Mar-Apr;8(2):148-50. doi: 10.1016/0887-8994(92)90039-2.

Incest and mental handicap.

J Ment Defic Res. 1990 Dec;34 ( Pt 6):483-90. doi: 10.1111/j.1365-2788.1990.tb01560.x.

Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus.

Arch Neurol. 1970 Sep;23(3):201-9. doi: 10.1001/archneur.1970.00480270011002.

Surgery in lower limbs in cerebral palsy.

Dev Med Child Neurol. 1972 Feb;14(1):45-50. doi: 10.1111/j.1469-8749.1972.tb02553.x.

引用本文的文献

Familial risk of cerebral palsy: population based cohort study.

BMJ. 2014 Jul 15;349:g4294. doi: 10.1136/bmj.g4294.

Genetic association study of adaptor protein complex 4 with cerebral palsy in a Han Chinese population.

Mol Biol Rep. 2013 Nov;40(11):6459-67. doi: 10.1007/s11033-013-2761-6. Epub 2013 Sep 25.

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CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592.

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An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation.

Am J Med Genet A. 2006 Jul 15;140(14):1504-10. doi: 10.1002/ajmg.a.31288.

BMC Neurol. 2004 Nov 30;4(1):20. doi: 10.1186/1471-2377-4-20.

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

Am J Hum Genet. 1999 Feb;64(2):526-32. doi: 10.1086/302237.

Genetic aspects of congenital cerebellar ataxia.

Indian J Pediatr. 1986 Nov-Dec;53(6):761-73. doi: 10.1007/BF02748571.

Familial cerebral palsy associated with normal intelligence.

Postgrad Med J. 1986 Sep;62(731):827-30. doi: 10.1136/pgmj.62.731.827.

Epidemiological and preventive aspects of cerebral palsy and severe mental retardation in Sweden.

Eur J Pediatr. 1979 Feb 8;130(2):71-8. doi: 10.1007/BF00442344.