Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies

J Craniofac Genet Dev Biol. Oct-Dec 1992;12(4):196-244.

Abstract

This paper presents an updated analytic review of the holoprosencephalic disorders. Central nervous system findings and craniofacial anatomy are discussed in depth. Associated anomalies and syndromes are updated with a syndrome commentary that attempts to separate durable syndromes from associated anomalies and spurious entities. The differential diagnosis of various conditions that may simulate the holoprosencephalic disorders is also discussed. Various experimental approaches to holoprosencephaly are reviewed, indicating that holoprosencephaly appears to be both etiologically and pathogenetically heterogeneous.

Publication types

  • Review

MeSH terms

  • Animals
  • Central Nervous System / abnormalities*
  • Central Nervous System / embryology
  • Chromosomes, Human, Pair 13
  • Chromosomes, Human, Pair 7
  • Chromosomes, Human, Pair 8
  • Diagnosis, Differential
  • Facial Bones / abnormalities*
  • Holoprosencephaly / diagnosis*
  • Holoprosencephaly / etiology
  • Holoprosencephaly / genetics
  • Humans
  • Skull / abnormalities*
  • Tomography, X-Ray Computed