Review
doi: 10.1002/ajmg.1320340232.
Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities
Affiliations
- PMID: 2683788
- DOI: 10.1002/ajmg.1320340232
Item in Clipboard
Review
Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities
Am J Med Genet.
1989 Oct.
Abstract
This paper attempts to balance our knowledge of holoprosencephalic spectra and continuities with important distinctions and discontinuities. Prevalence studies and syndrome delineation are briefly reviewed. The following topics receive detailed coverage: human teratogens, special aspects of forebrain and hindbrain malformations, aprosencephaly/atelencephaly, association with neural tube defects, current assessment of "facial principles," and endocrine abnormalities.
Comment in
-
Agenesis of the nasal septal cartilage: another sign in autosomal dominant holoprosencephaly.Am J Med Genet. 1991 Apr 1;39(1):121-2. doi: 10.1002/ajmg.1320390127. Am J Med Genet. 1991. PMID: 1844347 No abstract available.
-
Holoprosencephaly as a possible embryonic alcohol effect: another observation.Am J Med Genet. 1990 Nov;37(3):431-2. doi: 10.1002/ajmg.1320370328. Am J Med Genet. 1990. PMID: 2260579 No abstract available.
Similar articles
-
Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.Teratology. 1989 Sep;40(3):211-35. doi: 10.1002/tera.1420400304. Teratology. 1989. PMID: 2688166 Review.
-
Atelencephalic microcephaly: craniofacial anatomy and morphologic comparisons with holoprosencephaly and anencephaly.Teratology. 1987 Dec;36(3):279-85. doi: 10.1002/tera.1420360302. Teratology. 1987. PMID: 3424215
-
Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies.J Craniofac Genet Dev Biol. 1992 Oct-Dec;12(4):196-244. J Craniofac Genet Dev Biol. 1992. PMID: 1494025 Review.
-
Microscopic study of holoprosencephalic facial anomalies in trisomy 13 fetuses.Am J Med Genet. 1989 Apr;32(4):443-51. doi: 10.1002/ajmg.1320320402. Am J Med Genet. 1989. PMID: 2773983
-
Acalvaria, holoprosencephaly, and facial dysmorphism syndrome.J Craniofac Genet Dev Biol Suppl. 1986;2:319-29. J Craniofac Genet Dev Biol Suppl. 1986. PMID: 3491120
Cited by
-
Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.
-
Spectrum of holoprosencephaly.Indian J Pediatr. 2004 Jul;71(7):593-7. doi: 10.1007/BF02724118. Indian J Pediatr. 2004. PMID: 15280608
-
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.J Med Genet. 1993 Sep;30(9):713-27. doi: 10.1136/jmg.30.9.713. J Med Genet. 1993. PMID: 8411066 Free PMC article. Review. No abstract available.
-
Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephaly.J Med Genet. 1997 Nov;34(11):899-903. doi: 10.1136/jmg.34.11.899. J Med Genet. 1997. PMID: 9391882 Free PMC article.
-
Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephaly.Arch Dis Child. 2002 Apr;86(4):293-6. doi: 10.1136/adc.86.4.293. Arch Dis Child. 2002. PMID: 11919111 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources