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• Lysosomal storage diseases
  ...ximately 50 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large mole The term "lysosomal storage diseases" was coined in the late 20th century. The word "lysosome"
  2 KB (234 words) - 21:40, 13 February 2024
• Lysosomal storage disease
  '''Lysosomal storage disease''' (''pronunciation: ly·​so·​so·​mal stor·​age ...tely 50 rare inherited [[metabolic disorders]] that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large mole
  2 KB (224 words) - 02:41, 12 February 2024
• Lysosomal storage disorder
  == Lysosomal Storage Disorder == ...abolic disorders that result from defects in lysosomal function. The term "lysosomal storage disorder" is derived from the Greek words "lysis" which means "loos
  2 KB (277 words) - 04:20, 12 February 2024
• Lysosomal acid lipase deficiency
  == Lysosomal Acid Lipase Deficiency == ...c disorder]] that affects the body's ability to produce an enzyme called [[lysosomal acid lipase]] (LAL). The term originates from the Greek words "lysis" meani
  2 KB (282 words) - 19:46, 7 February 2024

Page text matches

• Wolman disease
  #REDIRECT [[Lysosomal acid lipase deficiency]]
  46 bytes (5 words) - 19:40, 3 February 2024
• Cholesteryl ester storage disease
  #REDIRECT [[Lysosomal acid lipase deficiency]]
  46 bytes (5 words) - 20:15, 3 February 2024
• Lysosomal storage diseases
  ...ximately 50 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large mole The term "lysosomal storage diseases" was coined in the late 20th century. The word "lysosome"
  2 KB (234 words) - 21:40, 13 February 2024
• Lysosomal storage disorder
  == Lysosomal Storage Disorder == ...abolic disorders that result from defects in lysosomal function. The term "lysosomal storage disorder" is derived from the Greek words "lysis" which means "loos
  2 KB (277 words) - 04:20, 12 February 2024
• Lysosomal storage disease
  '''Lysosomal storage disease''' (''pronunciation: ly·​so·​so·​mal stor·​age ...tely 50 rare inherited [[metabolic disorders]] that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large mole
  2 KB (224 words) - 02:41, 12 February 2024
• Chaperone-mediated autophagy
  ...]] that involves the direct translocation of cytosolic proteins across the lysosomal membrane for degradation. ...otein into the lysosome. Inside the lysosome, the protein is degraded by [[lysosomal hydrolases]].
  2 KB (265 words) - 23:05, 14 February 2024
• Sebelipase alfa
  ...lipase enzyme. It is used as a replacement therapy for the treatment of [[lysosomal acid lipase deficiency]] (LAL-D), a rare genetic disorder. ...enetic disorder that prevents the body from producing enough of the enzyme lysosomal acid lipase. This enzyme is necessary for the breakdown and removal of cert
  2 KB (224 words) - 19:49, 9 February 2024
• Dysostosis multiplex
  ...bnormalities that are often seen in individuals with certain metabolic and lysosomal storage disorders. The term is derived from the Greek words ''dys'' meaning ...accharidoses|Mucopolysaccharidosis]] and other [[Lysosomal storage disease|lysosomal storage disorders]].
  2 KB (263 words) - 06:05, 11 February 2024
• Lysosomal acid lipase deficiency
  == Lysosomal Acid Lipase Deficiency == ...c disorder]] that affects the body's ability to produce an enzyme called [[lysosomal acid lipase]] (LAL). The term originates from the Greek words "lysis" meani
  2 KB (282 words) - 19:46, 7 February 2024
• Substrate reduction therapy
  ...re-duck-shun ther-uh-pee) is a form of [[treatment]] used primarily for [[lysosomal storage diseases]]. Substrate reduction therapy is used in the treatment of several lysosomal storage diseases, including [[Gaucher's disease]], [[Tay-Sachs disease]], a
  2 KB (231 words) - 04:15, 12 February 2024
• Pseudo-Hurler polydystrophy
  ...udo-Hurler" is derived from its similarity to [[Hurler syndrome]], another lysosomal storage disorder. "Polydystrophy" refers to the multiple organ systems that * [[Lysosomal storage disorder]]
  2 KB (230 words) - 14:42, 11 February 2024
• Beta-mannosidosis
  '''Beta-mannosidosis''' (pronounced: be-ta-man-no-si-do-sis) is a rare [[lysosomal storage disorder]] characterized by the body's inability to break down cert * [[Lysosomal storage disorder]]
  2 KB (245 words) - 01:37, 8 February 2024
• Maroteaux–Lamy syndrome
  ...type VI]]''' (MPS VI) or '''[[Arylsulfatase B]] deficiency''', is a rare [[lysosomal storage disease]] characterized by a deficiency of the enzyme arylsulfatase * [[Lysosomal storage disease]]
  2 KB (271 words) - 19:46, 7 February 2024
• Galactosialidosis
  Galactosialidosis is a [[lysosomal storage disease]] characterized by a combined deficiency of [[beta-galactos * [[Lysosomal storage disease]]
  2 KB (270 words) - 01:53, 8 February 2024
• Alpha-mannosidosis
  '''Alpha-mannosidosis''' (pronounced: al-fa-man-o-si-do-sis) is a rare [[lysosomal storage disorder]] characterized by the body's inability to break down cert * [[Lysosomal storage disorder]]
  2 KB (271 words) - 01:50, 8 February 2024
• Danon disease
  '''Danon Disease''' (pronounced: /ˈdænɒn/), also known as '''Lysosomal Glycogen Storage Disease Type IIb''', is a rare genetic disorder characteri ...anon]], who first described the condition. The disease is also known as '''Lysosomal Glycogen Storage Disease Type IIb''' due to its association with the accumu
  2 KB (307 words) - 22:43, 8 February 2024
• Hurler
  ...' (MPS I), is a rare genetic disorder characterized by a deficiency of the lysosomal enzyme alpha-L-iduronidase. This deficiency leads to an accumulation of spe * [[Lysosomal storage disease]]
  1 KB (177 words) - 16:25, 4 February 2024
• Hurler–Scheie syndrome
  Hurler–Scheie syndrome is a lysosomal storage disease caused by a deficiency in the enzyme [[alpha-L-iduronidase] * [[Lysosomal storage disease]]
  2 KB (277 words) - 20:10, 7 February 2024
• Filipin
  ...is particularly useful in the study of [[Niemann-Pick disease]], a type of lysosomal storage disease, as it can bind to unesterified cholesterol in cells, allow * [[Niemann-Pick disease]]: A type of lysosomal storage disease that is characterized by the accumulation of cholesterol in
  1 KB (188 words) - 23:28, 4 February 2024
• Wolman's disease
  Wolman's disease is a severe form of [[lysosomal storage disease]] characterized by the complete absence or near-absence of * [[Lysosomal storage disease]]
  2 KB (293 words) - 22:56, 9 February 2024

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