Literature DB >> 6827707

Family studies in tuberous sclerosis. evaluation of apparently unaffected parents.

S B Cassidy, R A Pagon, M Pepin, J D Blumhagen.   

Abstract

A family study was conducted to evaluate the apparently unaffected parents of 13 patients with tuberous sclerosis. None of the parents had a personal or family history suggesting the diagnosis of tuberous sclerosis. All 26 parents were examined according to a protocol that entailed medical history, physical examination (including Wood's lamp examination of the skin), funduscopic examination through a dilated pupil, roentgenograms of the hands, feet, and skull, renal ultrasound studies, and cranial computed tomography (CT). In these 13 families, three fathers and one mother had previously undiagnosed tuberous sclerosis. Three of the four had skin changes, three had calcifications shown by CT, and one had renal cysts. These data demonstrate the importance of detailed examination of all parents of patients with tuberous sclerosis before recurrence-risk counseling is given.

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Year:  1983        PMID: 6827707

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  11 in total

1.  Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.

Authors:  H Northrup; D J Kwiatkowski; E S Roach; W B Dobyns; R A Lewis; G E Herman; E Rodriguez; S P Daiger; S H Blanton
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

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

Review 3.  Diagnosis of tuberous sclerosis.

Authors:  J P Osborne
Journal:  Arch Dis Child       Date:  1988-12       Impact factor: 3.791

4.  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

5.  Unsuccessful attempt to detect genetic mutation in tuberous sclerosis utilizing the polymerase chain reaction.

Authors:  R Watanabe; M Ebihara; F Otsuka; K Onodera; Y Ishibashi
Journal:  Arch Dermatol Res       Date:  1993       Impact factor: 3.017

6.  Tuberous sclerosis complex: diagnostic challenges, presenting symptoms, and commonly missed signs.

Authors:  Brigid A Staley; Emily A Vail; Elizabeth A Thiele
Journal:  Pediatrics       Date:  2010-12-20       Impact factor: 7.124

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: case study of early seizure control and subsequent normal development.

Authors:  V W Lane; J M Samples
Journal:  J Autism Dev Disord       Date:  1984-12

10.  Renal involvement in tuberous sclerosis complex: a retrospective survey.

Authors:  L B Zimmerhackl; M Rehm; K Kaufmehl; G Kurlemann; M Brandis
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714

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