Mid-diaphyseal Endosteal Thickening With Subsequent Medullary Narrowing in a Patient With Hallermann-Streiff Syndrome.

作者信息

Kaissi Ali Al, Handelbauer Albert, Klaushofer Klaus, Grill Franz

机构信息

Ludwig Boltzmann Institute of Osteology at the Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, First Medical Department, Hanusch Hospital, Vienna, Austria.

出版信息

J Clin Med Res. 2011 Dec;3(6):328-30. doi: 10.4021/jocmr704e. Epub 2011 Nov 10.

DOI:10.4021/jocmr704e

PMID:22393346

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3279479/

Abstract

UNLABELLED

We report on a 5-year-old girl who presented with the full clinical criteria of Hallermann-Streiff syndrome (HSS). Classically, overtubulation (thin and gracile) bones are the characteristic and constant features in HSS. Interestingly, our present patient manifested unusual mid-diaphyseal endosteal thickening with subsequent medullary narrowing (defective endosteal resorption). To the best of our knowledge no previous reports described such unusual feature in a patient with HSS.