Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 2000 Apr 4;66(5):1705–1709. doi: 10.1086/302898

The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.

G N Kavaslar 1, S Onengüt 1, O Derman 1, A Kaya 1, A Tolun 1
PMCID: PMC1378027  PMID: 10762554

Abstract

We studied a large consanguineous Anatolian family with children who exhibited hydranencephaly associated with microcephaly. The children were severely affected. This novel genetic disorder is autosomal recessive. We used autozygosity mapping to identify a locus at chromosome 16p13.3-12.1; it has a LOD score of 4.11. The gene locus is within a maximal 11-cM interval between markers D16S497 and D16S672 and within a minimal critical region of 8 cM between markers D16S748 and D16S490.

Full Text

The Full Text of this article is available as a PDF (304.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bolger G., Michaeli T., Martins T., St John T., Steiner B., Rodgers L., Riggs M., Wigler M., Ferguson K. A family of human phosphodiesterases homologous to the dunce learning and memory gene product of Drosophila melanogaster are potential targets for antidepressant drugs. Mol Cell Biol. 1993 Oct;13(10):6558–6571. doi: 10.1128/mcb.13.10.6558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cole S. P., Bhardwaj G., Gerlach J. H., Mackie J. E., Grant C. E., Almquist K. C., Stewart A. J., Kurz E. U., Duncan A. M., Deeley R. G. Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. Science. 1992 Dec 4;258(5088):1650–1654. doi: 10.1126/science.1360704. [DOI] [PubMed] [Google Scholar]
  3. Farag T. I., Teebi A. S., Al-Awadi S. A. Nonsyndromal anencephaly: possible autosomal recessive variant. Am J Med Genet. 1986 Jul;24(3):461–464. doi: 10.1002/ajmg.1320240308. [DOI] [PubMed] [Google Scholar]
  4. Farag T. I., al-Awadi S. A., Yassin S., el-Kassaby T. A., Jaefary S., Usha R., Uma R., Mady S. A., Fakhr M., Mannae M. Anencephaly: a vanishing problem in Bedouins? J Med Genet. 1989 Aug;26(8):538–539. doi: 10.1136/jmg.26.8.538-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Fathallah-Shaykh H., Wolf S., Wong E., Posner J. B., Furneaux H. M. Cloning of a leucine-zipper protein recognized by the sera of patients with antibody-associated paraneoplastic cerebellar degeneration. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3451–3454. doi: 10.1073/pnas.88.8.3451. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hoshino S., Miyazawa H., Enomoto T., Hanaoka F., Kikuchi Y., Kikuchi A., Ui M. A human homologue of the yeast GST1 gene codes for a GTP-binding protein and is expressed in a proliferation-dependent manner in mammalian cells. EMBO J. 1989 Dec 1;8(12):3807–3814. doi: 10.1002/j.1460-2075.1989.tb08558.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kim R. Y., Gasser R., Wistow G. J. mu-crystallin is a mammalian homologue of Agrobacterium ornithine cyclodeaminase and is expressed in human retina. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9292–9296. doi: 10.1073/pnas.89.19.9292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Lander E. S., Botstein D. Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. Science. 1987 Jun 19;236(4808):1567–1570. doi: 10.1126/science.2884728. [DOI] [PubMed] [Google Scholar]
  9. Longhurst T. J., O'Neill G. M., Harvie R. M., Davey R. A. The anthracycline resistance-associated (ara) gene, a novel gene associated with multidrug resistance in a human leukaemia cell line. Br J Cancer. 1996 Nov;74(9):1331–1335. doi: 10.1038/bjc.1996.545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Miller S. A., Dykes D. D., Polesky H. F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988 Feb 11;16(3):1215–1215. doi: 10.1093/nar/16.3.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Shaffer L. G., Marazita M. L., Bodurtha J., Newlin A., Nance W. E. Evidence for a major gene in familial anencephaly. Am J Med Genet. 1990 May;36(1):97–101. doi: 10.1002/ajmg.1320360119. [DOI] [PubMed] [Google Scholar]
  12. Yen S., MacMahon B. Genetics of anencephaly and spina bifida? Lancet. 1968 Sep 14;2(7568):623–626. doi: 10.1016/s0140-6736(68)90709-5. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES