{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,5,4]],"date-time":"2023-05-04T11:40:36Z","timestamp":1683200436690},"reference-count":21,"publisher":"Oxford University Press (OUP)","issue":"731","license":[{"start":{"date-parts":[[1986,9,1]],"date-time":"1986-09-01T00:00:00Z","timestamp":525916800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1986,9,1]]},"abstract":"<jats:title>Summary<\/jats:title>\n               <jats:p>We describe two families affected by a recessively transmitted familial cerebral palsy with onset in infancy. Two sisters in the first family have a severe spastic diplegia. The older sister also has mild mental retardation and hypothyroidism whilst the younger sister is of normal intelligence. Two brothers in the second family have a spastic quadriparesis, fifth finger camptodactyly and normal intelligence.<\/jats:p>","DOI":"10.1136\/pgmj.62.731.827","type":"journal-article","created":{"date-parts":[[2008,12,29]],"date-time":"2008-12-29T20:58:16Z","timestamp":1230584296000},"page":"827-830","source":"Crossref","is-referenced-by-count":6,"title":["Familial cerebral palsy associated with normal intelligence"],"prefix":"10.1093","volume":"62","author":[{"given":"N J","family":"Wild","sequence":"first","affiliation":[{"name":"The Regional Child Development Centre, Alder Hey Children's Hospital , Eaton Road, Liverpool, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L","family":"Rosenbloom","sequence":"additional","affiliation":[{"name":"The Regional Child Development Centre, Alder Hey Children's Hospital , Eaton Road, Liverpool, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[1986,9,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1111\/j.1600-0447.1959.tb07537.x","article-title":"Hereditary spastic paraplegia: a family with 10 injured","volume":"34","author":"AAGENAES, 0","year":"1959","unstructured":"AAGENAES, 0. (1959). Hereditary spastic paraplegia: a family with 10 injured. Acta Psychiatrica Neurologica Scandinavica, 34, 489.","journal-title":"Acta Psychiatrica Neurologica Scandinavica"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1016\/0021-9681(61)90077-7","article-title":"Familial cerebral palsy","volume":"13","author":"ADLER, E.","year":"1961","unstructured":"ADLER, E. (1961). Familial cerebral palsy. Journal ofChronic Disease, 13, 207.","journal-title":"Journal ofChronic Disease"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"1089","DOI":"10.1016\/S0140-6736(71)90402-8","article-title":"Mental retardation and spastic paraparesis in four of eight siblings","volume":"ii,","author":"ALLPORT, R.B.","year":"1971","unstructured":"ALLPORT, R.B. (1971). Mental retardation and spastic paraparesis in four of eight siblings. Lancet, ii, 1089.","journal-title":"Lancet"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"360","DOI":"10.1136\/adc.25.124.360","article-title":"A survey of400 cases of cerebral palsy in childhood","volume":"25","author":"ASHER, P.; SCHONELL, F.E.","year":"1950","unstructured":"ASHER, P. & SCHONELL, F.E. (1950). A survey of400 cases of cerebral palsy in childhood. Archives of Disease in Childhood, 25, 360.","journal-title":"Archives of Disease in Childhood"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"512","DOI":"10.1111\/j.1469-8749.1983.tb13798.x","article-title":"The development of children with congenital hypothyroidism","volume":"25","author":"BIRRELL, J.; FROST, G.J.; PARKIN, J.M.","year":"1983","unstructured":"BIRRELL, J., FROST, G.J. & PARKIN, J.M. (1983). The development of children with congenital hypothyroidism. Developmental Medicine and Child Neurology, 25, 512.","journal-title":"Developmental Medicine and Child Neurology"},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"454","DOI":"10.1016\/S0022-3476(57)80255-8","article-title":"Hereditary cerebral palsy: a preliminary report","volume":"50","author":"BLUMEL, J.; EVANS, E.B.; EGGERS, G.W.N.","year":"1957","unstructured":"BLUMEL, J., EVANS, E.B. & EGGERS, G.W.N. (1957). Hereditary cerebral palsy: a preliminary report. Journal of Pediatrics, 50, 454.","journal-title":"Journal of Pediatrics"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1111\/j.1399-0004.1970.tb01971.x","article-title":"A pedigree with essential myoclonus and genetic spastic oligophrenia","volume":"1","author":"BOOK, J.A.; SJOGREN, T.","year":"1970","unstructured":"BOOK, J.A. & SJOGREN, T. (1970). A pedigree with essential myoclonus and genetic spastic oligophrenia. Clinical Genetics, 1, 95.","journal-title":"Clinical Genetics"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1111\/j.1469-8749.1977.tb07968.x","article-title":"Recurrence risks in families of children with symmetrical spasticity","volume":"19","author":"BUNDEY, S.; GRIFFITHS, M.I.","year":"1977","unstructured":"BUNDEY, S. & GRIFFITHS, M.I. (1977). Recurrence risks in families of children with symmetrical spasticity. Developmental Medicine and Child Neurology, 19, 179.","journal-title":"Developmental Medicine and Child Neurology"},{"issue":"4","key":"ref_9","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/0303-8467(82)90026-9","article-title":"Recessively inherited 'pure' spastic paraplegia: case study","volume":"84","author":"DE, C.O.O.; M., I.F.; GABREELS, F.J.M.; RENIER, W.O.; COLON, E.J.; TER, H.A.A.R.; A, B.G.","year":"1982","unstructured":"DE COO, I.F.M., GABREELS, F.J.M., RENIER, W.O., COLON, E.J. & TER HAAR, B.G.A. (1982). Recessively inherited 'pure' spastic paraplegia: case study. Clinical Neurology and Neurosurgery, 84-4, 247.","journal-title":"Clinical Neurology and Neurosurgery"},{"issue":"34","key":"ref_10","first-page":"7","article-title":"Cerebral palsy in Iceland","volume":"43","author":"GUDMUNDSSON, K.R.","year":"1967","unstructured":"GUDMUNDSSON, K.R. (1967). Cerebral palsy in Iceland. Acta Neurologica Scandinavica, 43 (Suppl 34), 7.","journal-title":"Acta Neurologica Scandinavica"},{"key":"ref_11","author":"GUSTAVSON, K.H.; HAGBERG, B.; SANNER, G.","year":"1969","unstructured":"GUSTAVSON, K.H., HAGBERG, B. & SANNER, G. (1969)."},{"key":"ref_12","first-page":"165","article-title":"Eine sippe mit einfach-rezessiver diplegia spastica infantilis (littlescher krankheit) aus einem schweizer inzuchtgebiet","volume":"11","author":"HANHART, E.","year":"1936","unstructured":"HANHART, E. (1936). Eine sippe mit einfach-rezessiver diplegia spastica infantilis (littlescher krankheit) aus einem schweizer inzuchtgebiet, Der Erbarzt, 11, 165.","journal-title":"Der Erbarzt"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"871","DOI":"10.1136\/jnnp.44.10.871","article-title":"Hereditary 'pure' spastic paraplegia: a clinical and genetic study of 22 families","volume":"44","author":"HARDING, A.E.","year":"1981","unstructured":"HARDING, A.E. (1981). Hereditary 'pure' spastic paraplegia: a clinical and genetic study of 22 families. Journal of Neurology, Neurosurgery and Psychiatry, 44, 871.","journal-title":"Journal of Neurology, Neurosurgery and Psychiatry"},{"key":"ref_14","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1136\/adc.53.8.611","article-title":"Neurological abnormalities in patients treated for hypothyroidism from early life","volume":"53","author":"MACFAUL, R.; DORNER, S.; BRETT, E.M.; GRANT, D.B.","year":"1978","unstructured":"MACFAUL, R., DORNER, S., BRETT, E.M. & GRANT, D.B. (1978). Neurological abnormalities in patients treated for hypothyroidism from early life. Archives of Disease in Childhood, 53, 611.","journal-title":"Archives of Disease in Childhood"},{"key":"ref_15","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1017\/S1120962300023878","article-title":"Recessive familial spastic paraplegia with retinal degeneration","volume":"23","author":"MACRAE, W.; STIEFFEL, J.; TODOROV, A.B.","year":"1974","unstructured":"MACRAE, W., STIEFFEL, J. & TODOROV, A.B. (1974). Recessive familial spastic paraplegia with retinal degeneration. Acta Geneticae Medicae Gemellologiae (Roma), 23, 249.","journal-title":"Acta Geneticae Medicae Gemellologiae (Roma)"},{"key":"ref_16","first-page":"p.","article-title":"Mendelian Inheritance in Man","author":"McKUSICK, V.A.","year":"1978","unstructured":"McKUSICK, V.A. (1978). Mendelian Inheritance in Man, 5th edn. p. XLVI. The Johns Hopkins University Press: Baltimore.","edition":"5th edn"},{"key":"ref_17","article-title":"A clinical and genetic study of 1,280 cases of mental defect. Medical Research Council (London). Special Report Series, No. 229. (Reprinted in 1975 by the Institute for Research into Mental and Multiple Handicap)","author":"PENROSE, L.S.","year":"1938","unstructured":"PENROSE, L.S. (1938). A clinical and genetic study of 1,280 cases of mental defect. Medical Research Council (London). Special Report Series, No. 229. (Reprinted in 1975 by the Institute for Research into Mental and Multiple Handicap). 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The Clinical Delineation of Birth Defects: VI; Nervous System. Birth Defects Original Article Series VII (I): 216","author":"THURMON, T.F.; WALKER, B.A.","year":"1971","unstructured":"THURMON, T.F. & WALKER, B.A. (1971). Two distinct types of autosomal dominant spastic paraplegia. The Clinical Delineation of Birth Defects: VI; Nervous System. Birth Defects Original Article Series VII (I): 216. New York."},{"key":"ref_21","article-title":"Two kindreds with a sex-linked recessive form of spastic paraplegia. The Clinical Delineation of Birth","author":"THURMON, T.F.; WALKER, B.A.; SCOTT, C.I.; ABBOTT, M.H.","year":"1971","unstructured":"THURMON, T.F., WALKER, B.A., SCOTT, C.I. & ABBOTT, M.H. (1971). Two kindreds with a sex-linked recessive form of spastic paraplegia. 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