Difference between revisions of "Gaucher disease"

Jump to navigation Jump to search
1 byte removed ,  02:22, 29 November 2013
no edit summary
Line 28: Line 28:
| ClinDDx    =
| ClinDDx    =
}}
}}
'''Gaucher disease''' is the most common [[lysosomal storage diseases|lysosomal storage disease]].<ref name=pmid18466035>{{Cite journal  | last1 = Chen | first1 = M. | last2 = Wang | first2 = J. | title = Gaucher disease: review of the literature. | journal = Arch Pathol Lab Med | volume = 132 | issue = 5 | pages = 851-3 | month = May | year = 2008 | doi = 10.1043/1543-2165(2008)132[851:GDROTL]2.0.CO;2 | PMID = 18466035 }}</ref>
'''Gaucher disease''' is the most common [[lysosomal storage diseases|lysosomal storage disease]].<ref name=pmid18466035>{{Cite journal  | last1 = Chen | first1 = M. | last2 = Wang | first2 = J. | title = Gaucher disease: review of the literature. | journal = Arch Pathol Lab Med | volume = 132 | issue = 5 | pages = 851-3 | month = May | year = 2008 | doi = 10.1043/1543-2165(2008)132[851:GDROTL]2.0.CO;2 | PMID = 18466035 }}</ref> Despite being the most common in its grouping, it is still quite rare.


Despite being the most common in its grouping, it is still quite rare. Like most [[storage disorders]], it is inherited autosomal recessive; thus, it is seen more commonly in families where people are marry their cousins.  
Like most [[storage disorders]], it is inherited autosomal recessive; thus, it is seen more commonly in families where people are marry their cousins.  


==General==
==General==
48,436

edits

Navigation menu