Aicardi syndrome in a genotypic male

Ophthalmic Genetics

Volumn 29, Issue 4, 2008, Pages 181-183

  Chappelow, Aimee V ^a   Reid, Janet ^a   Parikh, Sumit ^a   Traboulsi, Elias I ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Aicardi syndrome; Corpus callosum; Lacunae; Male; Retina; Seizures

Indexed keywords

AICARDI SYNDROME; ARTICLE; CASE REPORT; CAUCASIAN; CORPUS CALLOSUM AGENESIS; GENOTYPE; HUMAN; INFANTILE SPASM; KARYOTYPE 46,XY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOSCOPY; PRESCHOOL CHILD; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER; CONGENITAL MALFORMATION; CORPUS CALLOSUM; GENETICS; NEWBORN; OPTIC NERVE; RETINA DISEASE; SEIZURE; SEX CHROMOSOME ABERRATION; SYNDROME; X CHROMOSOME;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, X; CORPUS CALLOSUM; GENOTYPE; HUMANS; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; OPTIC NERVE; RETINAL DISEASES; SEIZURES; SEX CHROMOSOME ABERRATIONS; SPASMS, INFANTILE; SYNDROME;

EID: 56149085018     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.1080/13816810802320209     Document Type: Article

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