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A survey of published reports failed to show an identical patient, despite various similar cases.<\/jats:p>","DOI":"10.1136\/jmg.27.10.635","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:11:11Z","timestamp":1226329871000},"page":"635-636","source":"Crossref","is-referenced-by-count":7,"title":["Acquired alopecia, mental retardation, short stature, microcephaly, and optic atrophy."],"prefix":"10.1136","volume":"27","author":[{"given":"R C","family":"Hennekam","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E G","family":"Renckens-Wennen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1990,10,1]]},"reference":[{"key":"ref_1","first-page":"172","article-title":"Universal alopecia and microcephaly in 4 siblings. 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Congenital alopecia, psychomotor retardation, and convulsions in two sibs of a consanguineous marriage. J Inher Metab Dis 1980;3:49-53.","journal-title":"J Inher Metab Dis"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1111\/j.1399-0004.1977.tb01271.x","article-title":"Universal pennanent alopecia, psychomotor epilepsy, pyorrhoea and mental subnormality","volume":"11","author":"Shokeir, M.H.K.","year":"1977","unstructured":"Shokeir MHK. Universal pennanent alopecia, psychomotor epilepsy, pyorrhoea and mental subnormality. Clin Genet 1977;11:13-7.","journal-title":"Clin Genet"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1136\/jmg.20.1.64","article-title":"A new alopecia\/mental retardation syndrome","volume":"20","author":"Baraitser, M.; Carter, C.O.; Brett, E.M.","year":"1983","unstructured":"Baraitser M, Carter CO, Brett EM. A new alopecia\/mental retardation syndrome. 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Int J7 Dermatol 1974;13:261-5.","journal-title":"Am J Hum Genet; A dominantly inherited syndrome of microcephaly, sparse hair, mental retardation, and seizures"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"286","DOI":"10.1136\/jmg.21.4.286","article-title":"Trichothiodystrophyneurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases","volume":"21","author":"King, M.D.; Gummer, C.L.; Stephenson, J.B.P.","year":"1984","unstructured":"King MD, Gummer CL, Stephenson JBP. Trichothiodystrophyneurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases. J Med Genet 1984;21:286-9.","journal-title":"J Med Genet"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1016\/0887-8994(87)90037-3","article-title":"Congenital alopecia, seizures and psychomotor retardation in three siblings","volume":"3","author":"Wessel, H.B.; Barmada, M.A.; Hashida, J.","year":"1987","unstructured":"Wessel HB, Barmada MA, Hashida J. 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