Literature DB >> 7318839

The Weaver syndrome: a rare type of primordial overgrowth.

F Majewski, M Ranke, H Kemperdick, E Schmidt.   

Abstract

A boy with primordial overgrowth, macrocephaly, and anomalies of the face, nails, feet and skeleton is reported. Two cases in the literature- referred to as Weaver syndrome- exhibited nearly identical anomalies. All three cases were sporadic. Main symptoms of the Weaver syndrome are increased birth weight, early overgrowth, macrocephaly, accelerated osseous maturation, typical facies, hoarse, low pitched voice, hypertonia of muscles and mild developmental delay. Further symptoms are thin, deep-set nails, talipes equinovarus, widened distal femora, and some minor abnormalities. A second boy with primordial overgrowth and macrocephaly demonstrated some, but not all, the symptoms of this syndrome. Whether this boy showed a milder expression of the Weaver syndrome or benign familial macrocephaly is discussed.

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Year:  1981        PMID: 7318839     DOI: 10.1007/bf00443257

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  6 in total

1.  Benign familial macrocephaly: report of a family and review of the literature.

Authors:  A J Asch; G J Myers
Journal:  Pediatrics       Date:  1976-04       Impact factor: 7.124

2.  Marshall-Smith syndrome with large bifrontal diameter, broad distal femora, camptodactly, and without broad middle phalanges.

Authors:  T Shimura; Y Utsumi; S Fujikawa; H Nakamura; K Baba
Journal:  J Pediatr       Date:  1979-01       Impact factor: 4.406

3.  A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly.

Authors:  D D Weaver; C B Graham; I T Thomas; D W Smith
Journal:  J Pediatr       Date:  1974-04       Impact factor: 4.406

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Authors:  H G Schlack; R A Pfeiffer
Journal:  Munch Med Wochenschr       Date:  1970-01-02

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Authors:  S D Flatz; J Natzschka
Journal:  Klin Padiatr       Date:  1978-11       Impact factor: 1.349

6.  Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases.

Authors:  A L Kosseff; J Herrmann; E F Gilbert; C Viseskul; M Lubinsky; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-10-01       Impact factor: 3.183

  6 in total
  5 in total

1.  Weaver syndrome.

Authors:  T R Cole; N R Dennis; H E Hughes
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

2.  Autosomal dominant inheritance of Weaver syndrome.

Authors:  A Fryer; C Smith; L Rosenbloom; T Cole
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

3.  The Weaver syndrome in a girl.

Authors:  P Meinecke; E Schaefer; R Engelbrecht
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183

4.  A girl with the Weaver syndrome.

Authors:  E M Thompson; S Hill; J V Leonard; M E Pembrey
Journal:  J Med Genet       Date:  1987-04       Impact factor: 6.318

5.  Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Authors:  K Zerres; S Rudnik-Schöneborn; F Deget
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

  5 in total

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