Storage diseases

Storage diseases, also storage disorders, are a group of abnormalities where something abnormal accumulates. They arise from inborn errors of metabolism.

Most are inherited autosomal recessive.^[1]^[2]^[3]

Types

References

↑ Kloska, A.; Tylki-Szymańska, A.; Wegrzyn, G. (2011). "[Lysosomal storage diseases--an overview].". Postepy Biochem 57 (2): 128-32. PMID 21913413.
↑ van der Ploeg, AT.; Reuser, AJ. (Oct 2008). "Pompe's disease.". Lancet 372 (9646): 1342-53. doi:10.1016/S0140-6736(08)61555-X. PMID 18929906.
↑ Chen, M.; Wang, J. (May 2008). "Gaucher disease: review of the literature.". Arch Pathol Lab Med 132 (5): 851-3. doi:10.1043/1543-2165(2008)132[851:GDROTL]2.0.CO;2. PMID 18466035.

[1] Kloska, A.; Tylki-Szymańska, A.; Wegrzyn, G. (2011). "[Lysosomal storage diseases--an overview].". Postepy Biochem 57 (2): 128-32. PMID 21913413.

[2] van der Ploeg, AT.; Reuser, AJ. (Oct 2008). "Pompe's disease.". Lancet 372 (9646): 1342-53. doi:10.1016/S0140-6736(08)61555-X. PMID 18929906.

[pmid18466035-3] Chen, M.; Wang, J. (May 2008). "Gaucher disease: review of the literature.". Arch Pathol Lab Med 132 (5): 851-3. doi:10.1043/1543-2165(2008)132[851:GDROTL]2.0.CO;2. PMID 18466035.

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Storage diseases

Types

References

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