Microlissencephaly with cardiac, spinal and urogenital defects

Clinical Dysmorphology

Volumn 10, Issue 3, 2001, Pages 203-208

  Gardner, R J M ^a   Savarirayan, R ^a   Dunne, K B ^a   McLellan, J A ^a   Coleman, L T ^a   Suthers, G K ^b  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b WOMEN S AND CHILDREN S HOSPITAL   (Australia)

Author keywords

Lissencephaly; Microcephaly; Microlissencephaly; Valproate embryopathy

Indexed keywords

VALPROIC ACID;

AGYRIA; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRAIN SCINTISCANNING; CASE REPORT; CLINICAL FEATURE; FETUS; HEART DISEASE; HUMAN; MALE; MICROCEPHALY; NEWBORN; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SPINE MALFORMATION; SYNDROME; TERATOGENESIS; UROGENITAL TRACT MALFORMATION;

EID: 0034961955     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200107000-00010     Document Type: Article

References (5)

1. Microlissencephaly: A heterogeneous malformation of cortical development
2. Agenesis of the corpus callosum, infantile spasms, spastic quadriplegia, microcephaly and severe mental retardation in three siblings
3. Fetal valproate syndrome
4. A clinical study of 57 children with fetal anticonvulsant syndromes
5. A new autosomal recessive malformation syndrome involving the brain, retina, spine, heart, kidneys and genitalia