Literature DB >> 7632532

A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosis.

E Pedagogos1, G Flanagan, D M Francis, G J Becker, D M Danks, R G Walker.   

Abstract

This paper reports an isolated case of the exceedingly rare cutaneo-skeletal condition craniomandibular dermatodysostosis, in which focal glomerular sclerosis and end-stage renal failure developed and renal transplantation was required.

Entities:  

Mesh：

Year:  1995        PMID： 7632532     DOI： 10.1007/bf02254211

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


  10 in total

1.  [On a case of cleidocranial dysostosis].

Authors:  C CAVALLAZZI; R CREMONCINI; A QUADRI
Journal:  Riv Clin Pediatr       Date:  1960-04

2.  Another Italian family with mandibuloacral dysplasia: why does it seem more frequent in Italy?

Authors:  R Tenconi; F Miotti; A Miotti; G Audino; R Ferro; M Clementi
Journal:  Am J Med Genet       Date:  1986-06

3.  Osteo-onychodystrophy with nephropathy and renal osteodystrophy. A case report.

Authors:  K S Eisenberg; D E Potter; E G Bovill
Journal:  J Bone Joint Surg Am       Date:  1972-09       Impact factor: 5.284

4.  Renal disease in nail-patella syndrome: clinical and morphologic studies.

Authors:  J R Hoyer; A F Michael; R L Vernier
Journal:  Kidney Int       Date:  1972-10       Impact factor: 10.612

5.  Chondroitin-6-sulfate mucopoly-saccharidosis in conjunction with lymphopenia, defective cellular immunity and the nephrotic syndrome.

Authors:  R N Schimke; W A Horton; C R King; N L Martin
Journal:  Birth Defects Orig Artic Ser       Date:  1974

6.  Craniomandibular dermatodysostosis.

Authors:  D M Danks; V Mayne; N B Wettenhall; R K Hall
Journal:  Birth Defects Orig Artic Ser       Date:  1974

7.  Essential osteolysis with nephropathy. A review of the literature and case report of an unusual syndrome.

Authors:  J S Torg; H H Steel
Journal:  J Bone Joint Surg Am       Date:  1968-12       Impact factor: 5.284

8.  New syndrome manifested by mandibular hypoplasia, acroosteolysis, stiff joints and cutaneous atrophy (mandibuloacral dysplasia) in two unrelated boys.

Authors:  L W Young; J F Radebaugh; P Rubin; J A Sensenbrenner; G Fiorelli; V A McKusick
Journal:  Birth Defects Orig Artic Ser       Date:  1971-06

9.  Association of spondylo-epiphyseal dysplasia with nephrotic syndrome.

Authors:  J H Ehrich; G Offner; E Schirg; P F Hoyer; U Helmchen; J Brodehl
Journal:  Pediatr Nephrol       Date:  1990-03       Impact factor: 3.714

10.  Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from Montana.

Authors:  J M Opitz; R B Lowry; T M Holmes; K Morgan
Journal:  Am J Med Genet       Date:  1985-11
  10 in total
  1 in total

1.  A case report: Familial glucocorticoid deficiency associated with familial focal segmental glomerulosclerosis.

Authors:  Nanik Ram; Ali Asghar; Najmul Islam
Journal:  BMC Endocr Disord       Date:  2012-12-11       Impact factor: 2.763
  1 in total

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