Hyper-IgM syndrome type 4: Difference between revisions
Jump to navigation
Jump to search
m (Robot: Automated text replacement (-{{SIB}} + & -{{EH}} + & -{{EJ}} + & -{{Editor Help}} + & -{{Editor Join}} +)) |
m (Robot: Automated text replacement (-{{WikiDoc Cardiology Network Infobox}} +, -<references /> +{{reflist|2}}, -{{reflist}} +{{reflist|2}})) |
||
Line 19: | Line 19: | ||
==References== | ==References== | ||
{{reflist}} | {{reflist|2}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] |
Latest revision as of 18:23, 4 September 2012
Hyper-IgM syndrome type 4 | |
Immunoglobulin M | |
ICD-10 | D80.5 |
ICD-9 | 279.05 |
OMIM | 608184 |
eMedicine | ped/2457 |
MeSH | D053306 |
Hyper-IgM syndrome type 4 is a form of Hyper IgM syndrome which is a defect in class switch recombination downstream of the AICDA gene that does not impair Somatic Hyper Mutation.[1]
References
- ↑ Lougaris V, Badolato R, Ferrari S, Plebani A (2005). "Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features". Immunol. Rev. 203: 48–66. doi:10.1111/j.0105-2896.2005.00229.x. PMID 15661021.