https://www.thelancet.com/journals/langas/article/PIIS2468. 3/abstractLysosomal acid lipase deficiency is a rare, autosomal recessive condition caused

https://www.umcvc.org/health-library/nord1203CachedMar 2, 2016 . Wolman disease is a rare genetic disorder characterized by complete absence of

https://onlinelibrary.wiley.com/doi/full/10.1002/jcu.22481Apr 4, 2017 . No published case of Wolman's disease has described the prenatal sonographic

www.casereports.in/printerfriendly.aspx?id=184CachedSimilarThis leads to accumulation of cholesterol esters and triglycerides in multiple

https://www.preventiongenetics.com/testInfo.php?. Wolman+Disease. Disease. CachedWolman Disease and Cholesteryl Ester Storage Disease via the LIPA Gene.

https://globalgenes.org/. /darling-dakotas-life-taken-by-rare-lysosomal- storage-disorder-called-wolmans-disease/CachedSimilarIn October of 2009, Dakota was diagnosed with Wolman's disease. Wolman's

www.diseaseinfosearch.org/Wolman+disease/7523CachedWolman disease is a type of lysosomal storage disorder. It is an inherited

https://www.counsyl.com/diseases/lysosomal-acid-lipase-deficiency/CachedLAL deficiency likely represents a spectrum of disease, but sub-categories of the

https://pdfs.semanticscholar.org/. / 27062cbc48eb41e4d248e72f5a0e4388544a.pdfCachedAbstract. Cholesteryl ester storage disease (CESD, OMIM #278000) and Wolman

https://clinicaltrials.gov/ct2/show/NCT02383641CachedMar 9, 2015 . Wolman Disease Acid Lipase Deficiency Acid Cholesteryl Ester Hydrolase

https://jamanetwork.com/journals/jamapediatrics/fullarticle/505230Wolman disease occurred in a 2½-month-old Iranian girl. Besides the

https://academic.oup.com/ajcp/article/59/4/490/1764597Two additional cases of the acute infantile form of Wolman's disease, occurring in

ctgt.net/disorder/wolman-diseaseCachedLysosomal acid lipase deficiency also called as cholesteryl ester storage disease

www.jewishgeneticdiseases.org/diseases/wolman-disease-cholesteryl-ester- storage-disease/CachedWolman Disease / Cholesteryl Ester Storage Disease [LIPA]: An early-onset

https://www.news-medical.net/?tag=/Wolman-DiseaseCachedWolman Disease News and Research . (sebelipase alfa) as the first treatment

https://www.nature.com/articles/1702557Aug 25, 2000 . Wolman disease is characterized by severe diarrhea and malnutrition leading to death during infancy. Lysosomal acid lipase deficiency is the cause of the symptoms and signs. It is inherited in an autosomal recessive manner. All Wolman disease patients have adrenal gland calcification.

https://rarediseases.org/rare-diseases/wolman-disease/

https://rarediseases.org/rare-diseases/wolman-disease/CachedSimilarWolman disease is a type of lysosomal acid lipase (LAL) deficiency; a rare genetic disorder characterized by complete absence of an enzyme known as lysosomal acid lipase (LIPA or LAL). This enzyme is required to breakdown (metabolize) certain fats (lipids) in the body.

www.jlr.org/content/40/2/221.longWolman disease, associated with deficient hLAL activity, leads to massive

https://ommbid.mhmedical.com/content.aspx?aid=1102895045SimilarWolman disease has its onset in the first month postpartum with a progressive

https://medical-dictionary.thefreedictionary.com/Wolman+diseaseCachedLooking for online definition of Wolman disease in the Medical Dictionary?

https://www.researchgate.net/. /287739925_Wolman_disease_A_reviewRequest PDF on ResearchGate | Wolman disease: A review | Woman disease is

https://radiopaedia.org/articles/wolman-diseaseCachedSimilarWolman disease is a rare autosomal recessive inborn error of metabolism

https://ojrd.biomedcentral.com/articles/10.1186/s13023-017-0670-9CachedJun 28, 2017 . Neural stem cells for disease modeling of Wolman disease and evaluation of

https://en.wikipedia.org/wiki/Lysosomal_acid_lipase_deficiencyCachedSimilarLysosomal acid lipase deficiency also known as Wolman disease, is an

https://ghr.nlm.nih.gov/condition/lysosomal-acid-lipase-deficiencyCachedSimilarThe early-onset form was known as Wolman disease, and the later-onset form

https://rarediseases.info.nih.gov/diseases/7899/wolman-diseaseCachedSimilarWolman disease is a congenital disease characterized by an impaired metabolism of the fats (lipids). It is the most severe type of lysosomal acid lipase deficiency. The lysomal acid lipase deficiency causes a buildup of lipids (fats) in body organs and calcium deposits in the adrenal glands.

https://www.thelancet.com/journals/langas/article/PIIS2468. 3/fulltextWolman's disease can be considered the infantile (ie, early-onset) form of

https://www.healio.com/. disease/. /novel-therapy-increases-survival-in- infants-with-wolman-diseaseNov 7, 2017 . The study included 10 patients aged younger than 8 months with lysosomal acid

www.checkorphan.org/diseases/wolman-diseaseCachedWolman disease, Also known as early onset Lysosomal Acid Lipase (LAL)

https://www.merckmanuals.com/. /cholesteryl-ester-storage-disease-and- wolman-diseaseCachedCholesteryl Ester Storage Disease and Wolman Disease - Learn about the

www.dictionary.com/browse/wolman-s-diseaseCachedWolman's disease definition at Dictionary.com, a free online dictionary with

https://www.cedars-sinai.edu/Patients/Health. /Wolmans-Disease.aspxCachedSimilarA lysosomal storage disorder, Wolman's disease results in large amounts of

https://www.wideacademy.co/. /wolman-disease-and-the-future-of-treatment- using-stem-cells/CachedMar 8, 2018 . Wolman disease is a rare inherited metabolic disorder caused by a complete

pediatrics.aappublications.org/content/83/6/1074.2Abstract. Presently available information indicates that Wolman disease is due to

www.bloodjournal.org/content/129/6/803SimilarA diagnosis of Wolman disease (lysosomal acid esterase deficiency) was made

https://jmg.bmj.com/content/13/1/49Abstract. Amniocentesis was performed in the 15th week of a pregnancy at risk

purl.bioontology.org/ontology/MEDDRA/10053687CachedPreferred Name. Wolman's disease. ID. http://purl.bioontology.org/ontology/

https://www.coriell.org/0/Sections/Search/Sample_Detail.aspx?. CachedWOLMAN DISEASE . Repository, NIGMS Human Genetic Cell Repository.

journals.sagepub.com/doi/abs/10.1177/000992289503400406Wolman Disease and Its Treatment. Show all authors. Moshe Wolman, M.D..

https://appliedradiology.com/articles/wolman-diseaseCachedSimilarMar 16, 2017 . Wolman disease. By Tuan V. Dao, MD; Gerald A. Mandell, MD, FACR, FAAP,

https://www.sciencedirect.com/topics/medicine-and. /wolman-diseaseWolman disease (WD) is an autosomal recessive storage disorder caused by

https://www.disabled-world.com/disability/types/wolman-disease.phpCachedSimilarFeb 22, 2010 . Wolman disease is a form of rare and inherited condition that involves the

www.pathologyoutlines.com/topic/liverwolman.htmlCachedSimilarNov 14, 2017 . Liver and intrahepatic bile ducts - nontumor - Wolman disease.

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB. CachedWolman disease represents the most severe manifestation of lysosomal acid

https://www.humpath.com/spip.php?article3660CachedJun 8, 2004 . Definition: Wolman's disease is a rare autosomal recessive lysosomal storage

https://www.omim.org/entry/278000CachedSimilarDeficiency of lysosomal acid lipase causes 2 distinct phenotypes in humans:

https://www.centerwatch.com/clinical-trials/. /867/wolman-disease/CachedA listing of Wolman Disease medical research trials actively recruiting patient

https://link.springer.com/chapter/10.1007/978-3-211-99390-3_62This lysosomal storage disease is an autosomal recessively inherited disorder

www.medlink.com/article/wolman_diseaseCachedFeb 12, 2018 . This article includes discussion of Wolman disease, Wolman syndrome,

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