Difference between revisions of "Lysosomal acid lipase deficiency"
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'''Lysosomal acid lipase deficiency''', abbreviated as '''LAL-D''', is a [[lysosomal storage disorder]] that is inherited autosomal recessive.<ref>{{Cite journal | last1 = Reiner | first1 = Ž. | last2 = Guardamagna | first2 = O. | last3 = Nair | first3 = D. | last4 = Soran | first4 = H. | last5 = Hovingh | first5 = K. | last6 = Bertolini | first6 = S. | last7 = Jones | first7 = S. | last8 = Ćorić | first8 = M. | last9 = Calandra | first9 = S. | title = Lysosomal acid lipase deficiency--an under-recognized cause of dyslipidaemia and liver dysfunction. | journal = Atherosclerosis | volume = 235 | issue = 1 | pages = 21-30 | month = Jul | year = 2014 | doi = 10.1016/j.atherosclerosis.2014.04.003 | PMID = 24792990 }}</ref> | '''Lysosomal acid lipase deficiency''', abbreviated as '''LAL-D''', is a [[lysosomal storage disorder]] that is inherited autosomal recessive.<ref>{{Cite journal | last1 = Reiner | first1 = Ž. | last2 = Guardamagna | first2 = O. | last3 = Nair | first3 = D. | last4 = Soran | first4 = H. | last5 = Hovingh | first5 = K. | last6 = Bertolini | first6 = S. | last7 = Jones | first7 = S. | last8 = Ćorić | first8 = M. | last9 = Calandra | first9 = S. | title = Lysosomal acid lipase deficiency--an under-recognized cause of dyslipidaemia and liver dysfunction. | journal = Atherosclerosis | volume = 235 | issue = 1 | pages = 21-30 | month = Jul | year = 2014 | doi = 10.1016/j.atherosclerosis.2014.04.003 | PMID = 24792990 }}</ref> | ||
It is also known as '''Wolman disease'''. | |||
==General== | ==General== | ||