Literature DB >> 6159800

Tuberous sclerosis: the incidence of sporadic cases versus familial cases.

P Fleury, W P de Groot, J W Delleman, B Verbeeten, I M Frankenmolen-Witkiezwicz.   

Abstract

In 48 families in which tuberous sclerosis occurred, extensive examination presented almost the same incidence of sporadic cases as reported in previous studies. Although inspection of the skin and cranial computed tomography seem to be the most sensitive diagnostic tests available, negative results with these methods do not exclude the diagnosis. Estimation of alpha 2-macroglobulin serum level does not mean an extension of the diagnostic arsenal.

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Year:  1980        PMID: 6159800     DOI: 10.1016/s0387-7604(80)80031-3

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  11 in total

1.  Developmental enamel defects in tuberous sclerosis: a clinical genetic marker?

Authors:  N Flanagan; W J O'Connor; B McCartan; S Miller; J McMenamin; R Watson
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  The value of investigation for genetic counselling in tuberous sclerosis.

Authors:  A E Fryer; A H Chalmers; J P Osborne
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

3.  Genetic aspects of tuberous sclerosis in the west of Scotland.

Authors:  J R Sampson; S J Scahill; J B Stephenson; L Mann; J M Connor
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

4.  Pulmonary tuberous sclerosis treated with tamoxifen and progesterone.

Authors:  C J Westermann; A C Oostveen; S S Wagenaar; C Hilvering; S E Overbeek; D Verheijen-Breemhaar; B Corrin
Journal:  Thorax       Date:  1986-11       Impact factor: 9.139

5.  FAMILIAL INCIDENCE OF TUBEROUS SCLEROSIS: A Case Report.

Authors:  M Akhtar; H P Singh; A S Narayanaswamy; N Kumar
Journal:  Med J Armed Forces India       Date:  2017-06-26

Review 6.  Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.

Authors:  A C Jones; M M Shyamsundar; M W Thomas; J Maynard; S Idziaszczyk; S Tomkins; J R Sampson; J P Cheadle
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

7.  Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis.

Authors:  L I al-Gazali; R J Arthur; J T Lamb; H M Hammer; T P Coker; P N Hirschmann; J Gibbs; R F Mueller
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

8.  Tuberous sclerosis: case report and investigation of family members.

Authors:  R D Wilson; J G Hall; B C McGillivray
Journal:  Can Med Assoc J       Date:  1985-04-01       Impact factor: 8.262

9.  Tuberous sclerosis: a new estimate of prevalence within the Oxford region.

Authors:  A Hunt; R H Lindenbaum
Journal:  J Med Genet       Date:  1984-08       Impact factor: 6.318

10.  Electron microscopy as a means for carrier detection and genetic counselling in families at risk of tuberous sclerosis.

Authors:  I Hausser; I Anton-Lamprecht
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

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