Literature DB >> 25897835

Different presentations of mevalonate kinase deficiency: a case series.

Carlo De Pieri1, Andrea Taddio2, Antonella Insalaco3, Egidio Barbi1, Loredana Lepore1, Alessandro Ventura2, Alberto Tommasini1.   

Abstract

OBJECTIVES: We aimed to raise awareness among paediatricians and physicians about this often misunderstood condition.
METHODS: We discussed the clinical profiles associated with late or wrong diagnosis of mevalonate kinase deficency (MKD) in a single centre case series.
RESULTS: We analysed the most common challenges and pitfalls that a clinician might face during the diagnostic process. Five main clinical profiles were characterised.
CONCLUSIONS: We propose a new perspective on MKD, suggesting that the presentation of this disease can vary from patient to patient.

Entities:  

Mesh:

Year:  2015        PMID: 25897835

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  8 in total

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2.  MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency.

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8.  Vasculitis in a patient with mevalonate kinase deficiency (MKD): a case report.

Authors:  Ebun Omoyinmi; Dorota Rowczenio; Neil Sebire; Paul A Brogan; Despina Eleftheriou
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  8 in total

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