Literature DB >> 21655669

Holoprosencephaly sequence.

Elena Coletă1, Mirela Siminel, Mihaela Gheonea.   

Abstract

Holoprosencephaly (HPE) sequence is a rare spectrum of cerebral and facial malformations resulting from incomplete division of the embryonic forebrain into distinct lateral cerebral hemisphere. Three ranges of increasing severity are described: lobar, semi-lobar and alobar HPE. A subtype of HPE called middle inter-hemispheric variant (MIHF) has been also reported. The etiology is heterogeneous: teratogens, chromosomal abnormalities and single gene mutations can be involved. Holoprosencephaly results in early morbidity and mortality with a reduced survival beyond neonatal period. The disorder is estimated to occur in 1/16,000 live births. This case report presents a male new born diagnosed with holoprosencephaly, accompanied by median cleft palate, absent nasal bones and chromosomal abnormalities.

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Year:  2011        PMID: 21655669

Source DB:  PubMed          Journal:  Rom J Morphol Embryol        ISSN: 1220-0522            Impact factor:   1.033


  3 in total

1.  Holoprosencephaly in an Egyptian baby with ectrodactyly-ectodermal dysplasia-cleft syndrome: a case report.

Authors:  Kotb Abbass Metwalley Kalil; Hekma Saad Fargalley
Journal:  J Med Case Rep       Date:  2012-01-24

2.  A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia.

Authors:  Jeremy M Schraw; Renata H Benjamin; Daryl A Scott; Brian P Brooks; Robert B Hufnagel; Scott D McLean; Hope Northrup; Peter H Langlois; Mark A Canfield; Angela E Scheuerle; Christian P Schaaf; Joseph W Ray; Han Chen; Michael D Swartz; Laura E Mitchell; A J Agopian; Philip J Lupo
Journal:  Ophthalmic Epidemiol       Date:  2020-12-20

3.  Semilobar holoprosencephaly in a 12-month-old baby boy born to a primigravida patient with type 1 diabetes mellitus: a case report.

Authors:  Pedro Pallangyo; Frederick Lyimo; Paulina Nicholaus; Hilda Makungu; Maria Mtolera; Isaac Mawenya
Journal:  J Med Case Rep       Date:  2016-12-20
  3 in total

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