Literature DB >> 11851965

Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.

H G K Blaas1, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes.   

Abstract

OBJECTIVE: To investigate the prenatal appearance of the holoprosencephaly spectrum.
METHODS: A database of 1750 fetuses with congenital anomalies identified by ultrasound was prospectively collected from 1987 to 2000. Among them, 30 cases (1.7%) with holoprosencephaly were prenatally identified and described.
RESULTS: The prevalence of holoprosencephaly in the Health Region of the National Center for Fetal Medicine in Norway was 1.26 : 10 000; the sex distribution (male : female) was 1.4 : 1. Holoprosencephaly was found in one dichorionic twin pregnancy and one pair of conjoined twins. Among the 30 cases of holoprosencephaly, 18 were alobar, five were semilobar, two were lobar, two were lobar variants, and three were anencephalic. The facial features varied considerably. Sixty-seven per cent (20/30) had associated structural anomalies that were not related to the cerebral and facial holoprosencephaly condition. Thirty-seven per cent (11/30) had detectable chromosome aberrations and 23% (7/30) had nonchromosomal syndromal origin. The size or shape of the head was abnormal in 83% (25/30) of holoprosencephaly cases.
CONCLUSION: This study indicates that holoprosencephaly represents a heterogeneous entity with different etiologies and clinical appearances. The fact that holoprosencephaly features are found associated with particular conditions such as fronto-nasal dysplasia (2/30; 6.7%), agnathia-otocephaly (3/30; 10%), and anencephaly (3/30; 10%), suggests that these may be underreported conditions in other large holoprosencephaly series.

Entities:  

Mesh:

Year:  2002        PMID: 11851965     DOI: 10.1046/j.0960-7692.2001.00154.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  14 in total

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Journal:  Am J Med Genet C Semin Med Genet       Date:  2011-10-17       Impact factor: 3.908

Review 2.  Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.

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Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-02-15       Impact factor: 3.908

Review 3.  Prenatal neurologic anomalies: sonographic diagnosis and treatment.

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Journal:  Paediatr Drugs       Date:  2012-06-01       Impact factor: 3.022

4.  Magnetic resonance microscopy defines ethanol-induced brain abnormalities in prenatal mice: effects of acute insult on gestational day 7.

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5.  Semilobar Holoprosencephaly with Neurogenic Hypernatraemia: Two new cases.

Authors:  Hashim Javad; Saif Al-Yarubi; Alexander P Chacko; Dilip Sankhla; Amna Al-Futasi; Anas A Abdelmogheth; Mohamed El-Naggari
Journal:  Sultan Qaboos Univ Med J       Date:  2013-06-25

6.  Holoprosencephaly with multiple anomalies of the craniofacial bones-an autopsy report.

Authors:  E Aruna; V Kalyan Chakravarthy; D Naveen Chandar Rao; D Ranga Rao
Journal:  J Clin Diagn Res       Date:  2013-08-01

7.  Otocephaly: Agnathia- Microstomia-Synotia Syndrome- A Rare Congenital Anomaly.

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Journal:  J Clin Diagn Res       Date:  2015-09-01

Review 8.  Re-focusing on Agnathia-Otocephaly complex.

Authors:  C Dubucs; N Chassaing; C Sergi; M Aubert-Mucca; T Attié-Bitach; D Lacombe; C Thauvin-Robinet; S Arpin; M J Perez; C Cabrol; C P Chen; J Aziza; E Colin; J Martinovic; P Calvas; Julie Plaisancié
Journal:  Clin Oral Investig       Date:  2020-07-09       Impact factor: 3.573

Review 9.  Imaging the fetal central nervous system.

Authors:  B De Keersmaecker; F Claus; L De Catte
Journal:  Facts Views Vis Obgyn       Date:  2011

Review 10.  Trisomy 13, 18, 21, Triploidy and Turner syndrome: the 5T's. Look at the hands.

Authors:  G Witters; J Van Robays; C Willekes; A Coumans; H Peeters; W Gyselaers; J P Fryns
Journal:  Facts Views Vis Obgyn       Date:  2011
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