PARRY ROMBERG SYNDROME IN A PEDIATRIC PATIENT

Journal Title: IJSR-International Journal Of Scientific Research - Year 2017, Vol 6, Issue 5

Abstract

Parry Romberg Syndrome is a rare disorder of suspected Autoimmune Etiology. First Described by Parry in 1825 and Romberg in 1846. Eulenberg in 1871 termed it as Progressive facial hemi atrophy. e syndrome is characterised by slow atrophy involving one side of face. e affected individuals are normal at birth, with insidious atrophy progression in first two Decades of life.. We Report a unique case of 9 years girl with parry Romberg syndrome with no neurological sequalae but with hypo plastic maxillary bones, malocclusion of teeth, atrophy of tongue hepatosplenomegaly and failure to thrive.

Authors and Affiliations

Dr Rahul Gandhi, Dr PD Sharmar, Dr Jitender

Keywords

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  • EP ID EP333361
  • DOI -
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How To Cite

Dr Rahul Gandhi, Dr PD Sharmar, Dr Jitender (2017). PARRY ROMBERG SYNDROME IN A PEDIATRIC PATIENT. IJSR-International Journal Of Scientific Research, 6(5), 30-31. https://europub.co.uk/articles/-A-333361