Kohlschutter's syndrome: A method of a rare and progressive neuroectodermal illness; case report and review of literature;Das Kohlschutter-Syndrom - Beispiel einer seltenen progredienten neuroektodermalen Erkrankung. Fallbeschreibung und Literaturubersicht

Klinische Padiatrie

Volumn 208, Issue 5, 1996, Pages 271-275

  Wygold, Thorsten ^a   Kurlemann, Gerd ^a   Schuierer, Gerhard ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENESIS IMPERFECTA; ARTICLE; BRAIN ATROPHY; CASE REPORT; ELECTROENCEPHALOGRAM; HUMAN; INFANT; MENTAL DEFICIENCY; NEUROECTODERM; NUCLEAR MAGNETIC RESONANCE; SEIZURE; SYNDROME; BRAIN; CONGENITAL MALFORMATION; ELECTROENCEPHALOGRAPHY; FRONTAL LOBE EPILEPSY; GENETICS; MALE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PRESCHOOL CHILD; REVIEW; TOOTH DISCOLORATION;

AMELOGENESIS IMPERFECTA; BRAIN; CHILD, PRESCHOOL; ELECTROENCEPHALOGRAPHY; EPILEPSY, FRONTAL LOBE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MENTAL RETARDATION; NEUROLOGIC EXAMINATION; TOOTH DISCOLORATION;

EID: 0030227635     PISSN: 03008630     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1046481     Document Type: Article

References (4)

1. Christodoulou, J., R. Hall, S. Menahem, I. Hopkins, J. Rogers: A syndrome of epilepsy, dementia and amelogenesis imperfecta: genetic and clinical features. J. Med. Genet. 25 (1988) 827-830
2. Kohlschütter, A., D. Chappuis, C. Meter, O. Tönz, F. Vassela, N. Herschkowitz: Familial epilepsy and yellow teeth - a disease of the central nervous system associated with enamel hypoplasia. Helv. Paediatr. Acta 29 (1974) 283-294
3. Petermöller, M., J. Kunze, G. Groß-Selbeck: Kohlschütter Syndrome: Syndrome of epilepsy - dementia - amelogenesis imperfecta. Neuropediatrics 24 (1993) 337-338
4. Zlotogora, J., A. Fuks, J. Borochowitz, Y. Tal: Kohlschütter-Tönz syndrome: Epilepsy, dementia and amelogenesis imperfecta. Am. J. Med. Gen. 46 (1993) 453-454