Search results

Page title matches

• Lysosomal storage diseases
  '''Lysosomal storage diseases''' (''pronunciation: ly-so-so-mal stor-age dis-eases'') are a group of appr ...lysosomes break down or "loosen" molecules in the body. The term "storage diseases" refers to the accumulation of undigested molecules in the lysosomes.
  2 KB (234 words) - 21:40, 13 February 2024

Page text matches

• Lysosomal storage diseases
  '''Lysosomal storage diseases''' (''pronunciation: ly-so-so-mal stor-age dis-eases'') are a group of appr ...lysosomes break down or "loosen" molecules in the body. The term "storage diseases" refers to the accumulation of undigested molecules in the lysosomes.
  2 KB (234 words) - 21:40, 13 February 2024
• Glycogen Storage Disease
  |Term=Glycogen Storage Disease ...y in the liver and muscle tissue. There are many types of glycogen storage diseases that can cause problems in different parts of the body, including the liver
  806 bytes (119 words) - 02:50, 8 January 2023
• Lysosomal storage disease
  '''Lysosomal storage disease''' (''pronunciation: ly·​so·​so·​mal stor·​age dis·​ Lysosomal storage diseases are a group of approximately 50 rare inherited [[metabolic disorders]] that
  2 KB (224 words) - 02:41, 12 February 2024
• Glycogen storage disease type ii
  '''Glycogen Storage Disease Type II''' ...n the cells. It is part of a group of diseases known as [[Glycogen Storage Diseases]].
  2 KB (334 words) - 21:56, 13 February 2024
• Cord blood bank
  ...is a medical facility that specializes in the collection, processing, and storage of [[umbilical cord blood]] following childbirth. ...hematopoietic stem cells]], which have the potential to treat a variety of diseases.
  2 KB (295 words) - 19:53, 11 February 2024
• Substrate reduction therapy
  ...-uh-pee) is a form of [[treatment]] used primarily for [[lysosomal storage diseases]]. ...er's disease]], [[Tay-Sachs disease]], and [[Niemann-Pick disease]]. These diseases are characterized by the accumulation of certain substances in the body's c
  2 KB (231 words) - 04:15, 12 February 2024
• Lysosomal storage disorder
  == Lysosomal Storage Disorder == ...orders that result from defects in lysosomal function. The term "lysosomal storage disorder" is derived from the Greek words "lysis" which means "loosening" o
  2 KB (277 words) - 04:20, 12 February 2024
• Glycogen storage disease type II
  '''Glycogen Storage Disease Type II''' '''Glycogen storage disease type II''' (pronounced: gly-co-gen stor-age dis-ease type two), als
  2 KB (301 words) - 22:54, 14 February 2024
• Danon disease
  ...non Disease''' (pronounced: /ˈdænɒn/), also known as '''Lysosomal Glycogen Storage Disease Type IIb''', is a rare genetic disorder characterized by the triad ...escribed the condition. The disease is also known as '''Lysosomal Glycogen Storage Disease Type IIb''' due to its association with the accumulation of glycoge
  2 KB (307 words) - 22:43, 8 February 2024
• Acid lipase disease
  ...[[Wolman disease]] and [[Cholesteryl ester storage disease]] (CESD). These diseases are characterized by the buildup of fats in the body due to the deficiency ...n certain fats in the body. When this enzyme is deficient, it leads to the diseases known as Acid Lipase Disease.
  2 KB (290 words) - 22:23, 11 February 2024
• Inborn error of metabolism
  ...unciation: /ɪnbɔːrn ˈɛrər ɒv mɛtəˈbɒlɪzəm/) are a large class of [[genetic diseases]] involving disorders of [[metabolism]]. The majority are due to defects of ...lism]], [[fatty acid oxidation and mitochondrial metabolism]], [[lysosomal storage disorders]], and [[peroxisomal disorders]].
  2 KB (255 words) - 06:21, 12 February 2024
• Niemann Pick disease
  ...f inherited metabolic disorders, known collectively as [[lysosomal storage diseases]], in which harmful quantities of fatty substances, or lipids, accumulate i * [[Lysosomal storage disease]]
  2 KB (309 words) - 22:05, 11 February 2024
• Maroteaux–Lamy syndrome
  ...'' (MPS VI) or '''[[Arylsulfatase B]] deficiency''', is a rare [[lysosomal storage disease]] characterized by a deficiency of the enzyme arylsulfatase B. This * [[Lysosomal storage disease]]
  2 KB (271 words) - 19:46, 7 February 2024
• Enzyme replacement therapy
  ...are caused by the lack of a functional enzyme, such as [[Lysosomal storage diseases]] (LSDs) including [[Gaucher's disease]], [[Fabry disease]], and [[Pompe di * [[Lysosomal storage diseases]]
  2 KB (264 words) - 04:13, 12 February 2024
• Disease informatics
  ...Philippe Dreyfus in 1962. It refers to the science of processing data for storage and retrieval. ...es the collection, storage, analysis, and dissemination of data related to diseases and health conditions. This field plays a crucial role in epidemiology, pub
  2 KB (312 words) - 04:14, 11 February 2024
• Hurler–Scheie syndrome
  Hurler–Scheie syndrome is a lysosomal storage disease caused by a deficiency in the enzyme [[alpha-L-iduronidase]]. This * [[Lysosomal storage disease]]
  2 KB (277 words) - 20:10, 7 February 2024
• Lipid pneumonia
  ...ditions that cause fat to accumulate in the lungs, such as [[lipid storage diseases]]. * [[Lipid storage diseases]]
  2 KB (272 words) - 17:42, 9 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 two enzy * [[Lysosomal storage disease]]
  2 KB (293 words) - 22:56, 9 February 2024
• PACS
  ...cation System''', is a medical imaging technology that provides economical storage and convenient access to images from multiple modalities (source machines). ..., a major concern for large hospitals. The universal format for PACS image storage and transfer is [[DICOM]] (Digital Imaging and Communications in Medicine).
  2 KB (222 words) - 21:15, 3 February 2024
• Gaucher's disease
  * [[Lysosomal storage disease]] * [[Rare diseases]]
  2 KB (279 words) - 11:46, 10 February 2024

View (previous 20 | next 20) (20 | 50 | 100 | 250 | 500)