Hemiconvulsion-hemiplegia-epilepsy syndrome with 1q44 microdeletion: Causal or chance association

American Journal of Medical Genetics, Part A

Volumn 164, Issue 1, 2014, Pages 186-189

  Gupta, Rekha ^a   Agarwal, Meenal ^a   Boqqula, Vijay R ^a   Phadke, Rajendra V ^a   Phadke, Shubha R ^a  

^a SANJAY GANDHI POSTGRADUATE INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

1q44 microdeletion; Cytogenetic microarray (CMA); Hemiconvulsion hemiplegia epilepsy (HHE); Preaxial polydactyly

Indexed keywords

ARTICLE; BRAIN ATROPHY; CASE REPORT; CHILD; CHROMOSOME 1Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FEMALE; HEMICONVULSION HEMIPLEGIA SYNDROME; HEMIPLEGIA; HUMAN; HYPERTELORISM; MICROARRAY ANALYSIS; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PHYSICAL EXAMINATION; POLYDACTYLY; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE, EPILEPSY AND CONVULSION; BRAIN; CHROMOSOME 1; COMPARATIVE GENOMIC HYBRIDIZATION; EPILEPSY; FACIES; FOOT MALFORMATION; GENETICS; KARYOTYPE; PATHOLOGY; SEIZURES; SYNDROME;

BRAIN; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; COMPARATIVE GENOMIC HYBRIDIZATION; EPILEPSY; FACIES; FEMALE; FOOT DEFORMITIES, CONGENITAL; HEMIPLEGIA; HUMANS; KARYOTYPE; MAGNETIC RESONANCE IMAGING; PHENOTYPE; SEIZURES; SYNDROME;

EID: 84890802634     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36198     Document Type: Article

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