Literature DB >> 1552544

Correlation of skeletal muscle biopsy with phenotype in the familial macrocephaly syndromes.

J H DiLiberti1.   

Abstract

The muscle biopsy results from 14 children with macrocephaly and hypotonia/weakness were correlated with clinical findings compatible with any of the autosomal dominant macrocephaly syndromes. Thirteen of the 14 had evidence of lipid storage myopathy, either generalised or focal. All 13 had examinations consistent with either benign familial macrocephaly, Ruvalcaba-Myhre-Smith syndrome, or Bannayan-Zonana syndrome. These results suggest that all three of these disorders may represent phenotypic variability at a single genetic locus.

Entities:  

Mesh:

Year:  1992        PMID: 1552544      PMCID: PMC1015821          DOI: 10.1136/jmg.29.1.46

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


  7 in total

1.  Bannayan-Riley-Ruvalcaba syndrome: renaming three formerly recognized syndromes as one etiologic entity.

Authors:  M M Cohen
Journal:  Am J Med Genet       Date:  1990-02

2.  Lipomatosis, angiomatosis, and macrencephalia. A previously undescribed congenital syndrome.

Authors:  G A Bannayan
Journal:  Arch Pathol       Date:  1971-07

3.  Heredofamilial syndrome of mesodermal hamartomas, macrocephaly, and pseudopapilledema.

Authors:  M Dvir; S Beer; M Aladjem
Journal:  Pediatrics       Date:  1988-02       Impact factor: 7.124

4.  Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia.

Authors:  R H Ruvalcaba; S Myhre; D W Smith
Journal:  Clin Genet       Date:  1980-12       Impact factor: 4.438

5.  Needle muscle biopsy in infants and children.

Authors:  J H DiLiberti; A N D'Agostino; G Cole
Journal:  J Pediatr       Date:  1983-10       Impact factor: 4.406

6.  Macrocephaly with hamartomas: Bannayan-Zonana syndrome.

Authors:  J H Miles; J Zonana; J Mcfarlane; K A Aleck; E Bawle
Journal:  Am J Med Genet       Date:  1984-10

7.  A new lipid storage myopathy observed in individuals with the Ruvalcaba-Myhre-Smith syndrome.

Authors:  J H DiLiberti; A N D'Agostino; R H Ruvalcaba; J R Schimschock
Journal:  Am J Med Genet       Date:  1984-05
  7 in total
  1 in total

1.  Muscle hemangiomatosis presenting as a severe feature in a patient with the pten mutation: expanding the phenotype of vascular malformations in bannayan-riley-ruvalcaba syndrome.

Authors:  Y Soysal; T Acun; Cm Lourenço; W Marques; Mc Yakıcıer
Journal:  Balkan J Med Genet       Date:  2012-06       Impact factor: 0.519

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.