P02-005 - Overlap of FMF and HIDS in one Arabic family
In: Pediatric Rheumatology, Jg. 11 (2013-11-01)
Online
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Zugriff:
Familial Mediterranean Fever (FMF) is commonly reported in Arabs, whereas Hyper-IgD syndrome (HIDS) is rare. Moreover, the simultaneous presence of MEFV and MVK mutations segregating in the same family is exceedingly rare. We report here an Arabic family in whom a combination of complex MEFV mutations and an MVK mutation segregate producing variable clinical phenotypes.
Titel: |
P02-005 - Overlap of FMF and HIDS in one Arabic family
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Autor/in / Beteiligte Person: | Fathalla, Basil M. ; El-Shanti, Hatem ; Aly, A ; Aladbe, B ; Taha, Rowaida Z. ; Moussa, Taha |
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Zeitschrift: | Pediatric Rheumatology, Jg. 11 (2013-11-01) |
Veröffentlichung: | Springer Science and Business Media LLC, 2013 |
Medientyp: | unknown |
ISSN: | 1546-0096 (print) |
DOI: | 10.1186/1546-0096-11-s1-a112 |
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