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Morgagni syndrome

Introduction

Synonyms and keywords: Morel’s syndrome, Morel-Moore syndrome, Morgagni’s syndrome, Morgagni’s trias, Morgagni-Morel-Stewart syndrome, Stewart-Morel syndrome, Stewart-Morel-Morgagni syndrome, metabolic craniopathy

Overview

Overview

Morgagni Stewart Morel syndrome is a condition characterized by thickening of the frontal bone of the skull (hyperostosis frontalis interna), as well as obesity and excessive hair growth (hypertrichosis) in some individuals. Other signs and symptoms may include seizures, headaches, diabetes insipidus, and sex gland disturbances.

Historical Perspective

Historical Perspective

It was first described in 1765.[1]

Pathophysiology

Pathophysiology

Associated Conditions

Diagnosis

Diagnosis

Symptoms

Physical Examination

References

References

  1. ↑ 1.0 1.1 She R, Szakacs J (2004). “Hyperostosis frontalis interna: case report and review of literature”. Ann. Clin. Lab. Sci. 34 (2): 206–8. PMIDΒ 15228235.
  2. ↑ 2.0 2.1 Nallegowda M, Singh U, Khanna M, Yadav SL, Choudhary AR, Thakar A (2005). “Morgagni Stewart Morel syndrome–additional features”. Neurol India. 53 (1): 117–9. PMIDΒ 15805672. Unknown parameter |month= ignored (help)

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]