A spectrum of phenotypical expression of Neu-laxova syndrome: Three case reports and a review of the literature

Fetal and Pediatric Pathology

Volumn 29, Issue 2, 2010, Pages 108-119

  Coto Puckett, Wendy L ^a   Gilbert Barness, Enid ^b   Steelman, Charlotte K ^c   Stuart, Tami ^d   Robinson, Haynes B ^e   Shehata, Bahig M ^d  

^a CHILDREN'S HEALTHCARE OF ATLANTA   (United States)

^b UNIVERSITY OF SOUTH FLORIDA   (United States)

^c Children's Healthcare of Atlanta ^*  (United States)

^d EMORY UNIVERSITY   (United States)

^e AKRON CHILDREN'S HOSPITAL   (United States)

Author keywords

Ichthyosis; IUGR; Neu Laxova

Indexed keywords

ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHROMOSOME ANALYSIS; CLINICAL EXAMINATION; CLINICAL FEATURE; FEMALE; FETUS; HUMAN; MICROSCOPY; NEU LAXOVA SYNDROME; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; STILLBIRTH;

ABNORMALITIES, MULTIPLE; CENTRAL NERVOUS SYSTEM; CONSANGUINITY; CRANIOFACIAL ABNORMALITIES; ECTODERMAL DYSPLASIA; FEMALE; HUMANS; ICHTHYOSIS; MICROCEPHALY; NERVOUS SYSTEM MALFORMATIONS; PHENOTYPE; PREGNANCY; RARE DISEASES; STILLBIRTH; SYNDROME;

EID: 77950217224     PISSN: 15513815     EISSN: 15513823     Source Type: Journal    
DOI: 10.3109/15513811003620914     Document Type: Article

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