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Volumn 38, Issue 1, 2008, Pages 198-201

Case report: Autistic disorder in Kabuki syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ANEMIA; AORTA ARCH; AUTISM; BLOOD EXAMINATION; CASE REPORT; CESAREAN SECTION; CHROMOSOME ANALYSIS; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; ECHOLALIA; EYE DISEASE; FERTILIZATION IN VITRO; FOLLOW UP; HUMAN; INTELLIGENCE TEST; KABUKI MAKEUP SYNDROME; LETTER; MALE; NEUROLOGIC EXAMINATION; OTITIS MEDIA; PEER GROUP; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SPEECH DEVELOPMENT; SPEECH DISORDER; THYROID FUNCTION TEST; ZINC DEFICIENCY;

EID: 37849001109     PISSN: 01623257     EISSN: 15733432     Source Type: Journal    
DOI: 10.1007/s10803-007-0433-x     Document Type: Letter
Times cited : (9)

References (12)
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    • 3. Review
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  • 3
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    • Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome
    • Halal, F., Gledhill, R., & Dudkiewicz, A. (1989). Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome. American Journal of Medical Genetics, 33, 376-381.
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  • 4
    • 0030744001 scopus 로고    scopus 로고
    • Kabuki make-up (Niikawa-Kuroki) syndrome: Cognitive abilities and autistic features
    • Ho, H.H., & Eaves, L.C. (1997). Kabuki make-up (Niikawa-Kuroki) syndrome: Cognitive abilities and autistic features. Developmental Medicine and Child Neurology, 39, 487-490.
    • (1997) Developmental Medicine and Child Neurology , vol.39 , pp. 487-490
    • Ho, H.H.1    Eaves, L.C.2
  • 5
    • 0028903780 scopus 로고
    • Kabuki make-up (Niikawa-Kuroki) syndrome in the Byelorussian register of congenital malformations: Ten new observations
    • Ilyina, H., Lurie, I., & Naumtchik, I., et al. (1995). Kabuki make-up (Niikawa-Kuroki) syndrome in the Byelorussian register of congenital malformations: Ten new observations. American Journal of Medical Genetics, 56, 127-131.
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  • 6
    • 0019837311 scopus 로고
    • A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation
    • Kuroki, Y., Suzuki, Y., & Chyo, H., et al. (1981). A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation. Journal of Pediatrics, 99, 570-573.
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    • Kuroki, Y.1    Suzuki, Y.2    Chyo, H.3
  • 8
    • 0344308337 scopus 로고    scopus 로고
    • Unmasking Kabuki syndrome: Chromosome 8p22-8p23.1 duplication revealed by comparative genomic hybridization and BAC-FISH
    • Milunsky, J.M., & Huang, J.M. (2003). Unmasking Kabuki syndrome: Chromosome 8p22-8p23.1 duplication revealed by comparative genomic hybridization and BAC-FISH. Clinical Genetics, 64, 509-516.
    • (2003) Clinical Genetics , vol.64 , pp. 509-516
    • Milunsky, J.M.1    Huang, J.M.2
  • 10
    • 0019850335 scopus 로고
    • Kabuki make-up syndrome: A syndrome of mental retardation, unusual faces, large and protruding ears, and postnatal growth deficiency
    • Niikawa, N., & Matsuura, N. (1981). Kabuki make-up syndrome: A syndrome of mental retardation, unusual faces, large and protruding ears, and postnatal growth deficiency. Journal of Pediatrics, 99, 565-569.
    • (1981) Journal of Pediatrics , vol.99 , pp. 565-569
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  • 11
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    • Ohdo, S., Madokoro, H., & Sonoda, T., et al. (1985). Kabuki make-up syndrome (Niikawa-Kuroki syndrome) associated with congenital heart disease. Journal of Medical Genetics, 22, 126-127.
    • (1985) Journal of Medical Genetics , vol.22 , pp. 126-127
    • Ohdo, S.1    Madokoro, H.2    Sonoda, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.