메뉴 건너뛰기




Volumn 24, Issue 3, 2001, Pages 228-231

IFAP syndrome 'plus' seizures, mental retardation, and callosal hypoplasia

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN ATROPHY; CASE REPORT; CHILD; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CORPUS CALLOSUM AGENESIS; ELECTROENCEPHALOGRAM; GRAND MAL SEIZURE; GROWTH RETARDATION; HUMAN; ICHTHYOSIS; MALE; MENTAL DEFICIENCY; NAIL DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PHOTOPHOBIA; PRIORITY JOURNAL;

EID: 0035075247     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(00)00261-7     Document Type: Article
Times cited : (18)

References (14)
  • 7
    • 0005444530 scopus 로고
    • Familial congenital alopecia, epilepsy, mental retardation with unusual electroencephalograms
    • (1962) Proc Roy Soc Med , vol.55 , pp. 411-412
    • Moynahan, E.J.1
  • 11
    • 0005449099 scopus 로고    scopus 로고
    • Cáceres-Ríos H, Tamayo-Sánchez L, Duran-Mckinster C, Orozco MA, de la Luz Ruiz-Maldonado R. Keratitis, ichthyosis, and deafness (KID syndrome): Review of the literature and proposal of a new terminology. Pediatr Dermatol 1996;13:105-13.
  • 14
    • 0345517152 scopus 로고    scopus 로고
    • Linear lesions reflecting lyonization in women heterozygous for IFAP syndrome (ichthyosis follicularis with atrichia and photophobia)
    • (1999) Am J Med Genet , vol.85 , pp. 365-368
    • Konig, A.1    Happle, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.