Document Detail


Can syndromic macrocephaly be diagnosed in utero?
MedLine Citation:
PMID:  20734344     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
OBJECTIVES: To compare the outcomes of fetuses with apparently isolated macrocephaly and those with associated findings, and to compare prenatal findings with postnatal diagnoses in children with syndromic macrocephaly.
METHODS: We reviewed the files of all patients referred for suspected fetal macrocephaly, during a 10-year period from 2000, to a large prenatal diagnosis unit with expertise in fetal neurology counseling. Macrocephaly was defined as head circumference (HC) > 2 SDs of the norm. Patients with confirmed HC > 2 SD were identified and contacted, and their development was evaluated.
RESULTS: Adequate data for analysis were available for 98 patients, in 82 of whom the fetal macrocephaly was considered isolated (Group A), and in 16 of whom associated fetal anomalies were identified (Group B). Macrocephaly was diagnosed earlier in Group B patients (28.4 vs. 32.3 weeks, P = 0.069), and the HC in Group B patients was larger (Z-score 2.95 vs. 2.3, P < 0.001). From Group A there were 81 liveborn; one of whom was diagnosed as having infantile autism. From Group B, there were nine liveborn. The associated central nervous system findings, as demonstrated by ultrasound and magnetic resonance imaging, included mild ventriculomegaly, malformations of cortical development, callosal abnormalities, overdeveloped sulcation, large cavum septi pellucidi, large subarachnoid spaces, mega cisterna magna, periventricular pseudocyst, open operculum and vermian dysgenesis. Syndromic diagnosis was made in utero in five fetuses and after birth in three. In eight patients, associated malformations were confirmed after birth but a specific diagnosis was not reached.
CONCLUSIONS: When fetal macrocephaly is associated with other brain or systemic anomalies, syndromic macrocephaly can be diagnosed in utero. Fetuses with syndromic macrocephaly have a significantly larger HC, usually > 2.5 SD above the mean. Isolated macrocephaly, particularly when the HC is < 2.5 SD above the norm, may be clinically benign.
Authors:
G Malinger; D Lev; L Ben-Sira; C Hoffmann; M Herrera; F Viñals; H Vinkler; S Ginath; Y Biran-Gol; D Kidron; T Lerman-Sagie
Related Documents :
19621234 - Unassisted smothering in a pillow.
7625754 - No evidence for genomic imprinting in liveborn down syndrome patients.
20210634 - Living with moebius syndrome: adjustment, social competence, and satisfaction with life.
19297044 - A nation-wide epidemiological study of acute bovine respiratory disease in france.
6822484 - Catatonia associated with glutethimide withdrawal.
8651274 - A study of fraxe in mentally retarded individuals referred for fragile x syndrome (frax...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology     Volume:  37     ISSN:  1469-0705     ISO Abbreviation:  Ultrasound Obstet Gynecol     Publication Date:  2011 Jan 
Date Detail:
Created Date:  2010-12-24     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9108340     Medline TA:  Ultrasound Obstet Gynecol     Country:  England    
Other Details:
Languages:  eng     Pagination:  72-81     Citation Subset:  IM    
Affiliation:
Fetal Neurology Clinic, Edith Wolfson Medical Center, Holon, Israel. gmalinger@gmail.com
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  An aqueous extract of Curcuma longa (turmeric) rhizomes stimulates insulin release and mimics insuli...
Next Document:  Determination of paeoniflorin, calycosin-7-O-?-d-glucoside, ononin, calycosin and formononetin in ra...