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The acro-osteolysis syndrome: Morphologic and biochemical studies

  • David M. Brown
  • , David S. Bradford
  • , Robert J. Gorlin
  • , Robert J. Desnick
  • , Leonard O. Langer
  • , Jenifer Jowsey
  • , John J. Sauk

Research output: Contribution to journalArticlepeer-review

60 Scopus citations

Abstract

The acro-osteolysis syndrome consists of dissolution of terminal phalanges of the hands and feet, dolichocephaly with multiple wormian bones, delayed closure of cranial sutures, absence of frontal sinuses, a prominent occipital ridge, skeletal demineralization, vertebral and extremity fractures, joint laxity, and coarse hair. Studies of bone morphology reveal diminished bone density and bone formation. Osteoblasts have widely dilated smooth endoplasmic reticulum. It is postulated that an abnormality of a structural protein is the pathogenic basis of this disease.

Original languageEnglish
Pages (from-to)573-580
Number of pages8
JournalJournal of Pediatrics
Volume88
Issue number4 PART 1
DOIs
StatePublished - Apr 1976
Externally publishedYes

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