A Case of Adams-Oliver Syndrome

Abstract

Adams-Oliver Syndrome was first described in 1945. It is a rare condition which is characterized by stellate aplasia cutis congenita of the scalp and terminal transverse limb defects. Six causative genes have been identified to date: ARHGAP31, DOCK6, EOGT, RBPJ, NOTCH1, and DLL4.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Apr 15, 2019
Accession Number
AD1081632

Entities

People

  • Giselle Castillo
  • Janessa England
  • Shannan Mccann

Organizations

  • 59th Medical Wing

Tags

DTIC Thesaurus Topics

  • Arteries
  • Bandages
  • Congenital Heart Defects
  • Dermatologic Agents
  • Genetic Testing
  • Hypertension
  • Liver Diseases
  • Mutations
  • Neuroimaging
  • Pathologic Constriction

Fields of Study

  • Medicine

Readers

  • Housing Policy Studies in Military Families with Privatization and Telomerase Allowance Units, Multi-Family Housing, and Telomere Lengths.
  • Immunology and Pathology
  • Trauma Surgery or Emergency Medicine.