Child with overgrowth, pigmentary streaks, polydactyly, and intestinal lymphangiectasia: macrocephaly-cutis marmorata telangiectatica congenita syndrome or new disorder?

Am J Med Genet A. 2003 Jan 15;116A(2):184-7. doi: 10.1002/ajmg.a.10705.

Abstract

We report a male patient with increased birth weight and growth, cutis marmorata, macrocephaly, large hands and feet, thick subcutaneous tissues, postaxial polydactyly, linear skin hyperpigmentation following the lines of Blaschko, and intestinal lymphangiectasia. Although the findings resemble the recently defined macrocephaly cutis marmorata syndrome, some findings suggest that this might be a new disorder. Differential diagnosis are discussed, with a review of the literature.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Abnormalities, Multiple / pathology*
  • Craniofacial Abnormalities
  • Diagnosis, Differential
  • Growth Disorders / pathology*
  • Humans
  • Infant
  • Lymphangiectasis, Intestinal / pathology*
  • Male
  • Polydactyly / pathology*
  • Skin Abnormalities*
  • Syndrome
  • Telangiectasia, Hereditary Hemorrhagic / pathology