Literature DB >> 8182716

Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

B Z Garty1, B Eisenstein, J Sandbank, S Kaffe, R Dagan, N Gadoth.   

Abstract

Three sibs born to consanguineous parents had congenital nephrotic syndrome, microcephaly, and psychomotor retardation. Pathology of the kidneys showed diffuse mesangial sclerosis with deposits of IgG and C3 in the mesangium and glomerular basement membranes. All three children died before the age of 3 years. Of 19 published cases of children with the association of congenital nephrotic syndrome and microcephaly, only four had histological evidence of diffuse mesangial sclerosis, and two of their sibs probably had the same disease. The association of nephrotic syndrome owing to congenital diffuse mesangial sclerosis, microcephaly, and mental retardation appears to be a distinct syndrome with an autosomal recessive mode of inheritance.

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Year:  1994        PMID: 8182716      PMCID: PMC1049672          DOI: 10.1136/jmg.31.2.121

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  26 in total

1.  Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis.

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Journal:  Pediatr Nephrol       Date:  1991-07       Impact factor: 3.714

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Journal:  Acta Neuropathol       Date:  1972       Impact factor: 17.088

3.  Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs.

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Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

4.  Silent microcephaly: a distinct autosomal dominant trait.

Authors:  M L Ramírez; F Rivas; J M Cantú
Journal:  Clin Genet       Date:  1983-04       Impact factor: 4.438

5.  Histopathologic variability of the congenital nephrotic syndrome.

Authors:  E V Martul; M G Cuesta; I Churg
Journal:  Clin Nephrol       Date:  1987-10       Impact factor: 0.975

6.  Familial infantile nephrotic syndrome with ocular abnormalities.

Authors:  C Glastre; P Cochat; R Bouvier; S Colon; X Cottin; D Giffon; C Wright; F Dijoud; L David
Journal:  Pediatr Nephrol       Date:  1990-07       Impact factor: 3.714

7.  The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases.

Authors:  R Habib; C Loirat; M C Gubler; P Niaudet; A Bensman; M Levy; M Broyer
Journal:  Clin Nephrol       Date:  1985-12       Impact factor: 0.975

Review 8.  Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy.

Authors:  B G Cooperstone; A Friedman; B S Kaplan
Journal:  Am J Med Genet       Date:  1993-08-15

9.  [Heterogeneity of early onset nephrotic syndromes in infants (nephrotic syndrome "in infants"). Anatomical, clinical and genetic study of 37 cases].

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Journal:  Helv Paediatr Acta       Date:  1973-05

10.  Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder?

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Journal:  Arch Dis Child       Date:  1986-06       Impact factor: 3.791

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  5 in total

1.  Infantile nephrotic syndrome with microcephaly and global developmental delay: the Galloway Mowat Syndrome.

Authors:  Sriram Krishnamurthy; N G Rajesh; Ananthakrishnan Ramesh; Martin Zenker
Journal:  Indian J Pediatr       Date:  2011-12-03       Impact factor: 1.967

2.  Microcephaly and early-onset nephrotic syndrome--confusion in Galloway-Mowat syndrome.

Authors:  H Sano; A Miyanoshita; N Watanabe; Y Koga; Y Miyazawa; Y Yamaguchi; Y Fukushima; N Itami
Journal:  Pediatr Nephrol       Date:  1995-12       Impact factor: 3.714

3.  The contribution of ultrasound for the differential diagnosis of congenital and infantile nephrotic syndrome.

Authors:  Hanna Salame; Nash Damry; Katt Vandenhoudt; Michèle Hall; Fred E Avni
Journal:  Eur Radiol       Date:  2003-05-08       Impact factor: 5.315

4.  WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis.

Authors:  Y Yang; C Jeanpierre; G R Dressler; M Lacoste; P Niaudet; M C Gubler
Journal:  Am J Pathol       Date:  1999-01       Impact factor: 4.307

Review 5.  Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings.

Authors:  Maha A Al-Rakan; Manal D Abothnain; Muhammad T Alrifai; Majid Alfadhel
Journal:  BMC Ophthalmol       Date:  2018-06-22       Impact factor: 2.209

  5 in total

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