Jackson-Weiss syndrome: clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter.

We describe the clinical and radiological manifestations of the Jackson-Weiss syndrome (JWS) in a large South Australian kindred. Radiological abnormalities not previously described in the hands include coned epiphyses, distal and middle phalangeal hypoplasia, and carpal bone malsegmentation. New radiological findings in the feet include coned epiphyses, hallux valgus, phalangeal, tarso-navicular and calcaneonavicular fusions, and uniform absence of metatarsal fusions. Absence of linkage to eight markers along the short arm of chromosome 7 excluded allelism between JWS and Saethre-Chotzen syndrome at 7p21. No linkage was detected to D5S211, excluding allelism to another recently described cephalosyndactyly syndrome mapping to 5qter.

[1]  J. Mulliken,et al.  Newly recognized autosomal dominant disorder with craniosynostosis. , 1993, American journal of medical genetics.

[2]  J. Weber,et al.  Assignment of a gene locus involved in craniosynostosis to chromosome 5qter. , 1993, Human molecular genetics.

[3]  G. Gyapay,et al.  A second-generation linkage map of the human genome , 1992, Nature.

[4]  R. Winter,et al.  The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p. , 1992, Journal of medical genetics.

[5]  K. Grzeschik,et al.  GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families , 1991, Nature.

[6]  M. V. Van Dyke,et al.  A rapid method for the purification of deprotected oligodeoxynucleotides. , 1991, Nucleic acids research.

[7]  P. Kroisel,et al.  Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes. , 1990, Genomics.

[8]  K. Kinzler,et al.  GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity , 1990, Molecular and cellular biology.

[9]  J. Weber,et al.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. , 1989, American journal of human genetics.

[10]  J. Opitz,et al.  Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13. , 1988, American journal of medical genetics.

[11]  J. Gitschier,et al.  An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. , 1987, The New England journal of medicine.

[12]  M. Aricò,et al.  A family with the Saethre-Chotzen syndrome. , 1985, American journal of medical genetics.

[13]  G. Lathrop,et al.  Easy calculations of lod scores and genetic risks on small computers. , 1984, American journal of human genetics.

[14]  N. Tommerup,et al.  A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome. , 1983, American journal of medical genetics.

[15]  D. Bixler,et al.  On the classification of the acrocephalosyndactyly syndromes , 1977, Clinical genetics.

[16]  L. Weiss,et al.  Craniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindred. , 1976, The Journal of pediatrics.

[17]  S. Kreiborg,et al.  The Saethre-Chotzen syndrome. , 1972, Teratology.

[18]  J. Opitz,et al.  Craniosynostosis in the Amish , 1969 .

[19]  C. Blank Apert's syndrome (a type of acrocephalosyndactyly)–observations on a British series of thirty‐nine cases* , 1959, Annals of human genetics.

[20]  N. Morton Sequential tests for the detection of linkage. , 1955, American journal of human genetics.