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  1. Glossary | Victor A. McKusick - Profiles in Science 
    https://profiles.nlm.nih.gov/spotlight/jq/feature/glossary
    ... organism possesses. Hurler syndrome -- The prototype of the mucopolysaccharidosis type disorders, caused by a deficiency of the ...
  2. NLM Digital Collections - Genetic Nosology: Three Approaches 
    Publication: Produced: 21 October 1977
    resource.nlm.nih.gov/101584632X129
    ... 1B), nosologic progress has been greatest in the mucopolysaccharidoses, especially since 1960. Tracing these advances may serve ... Disorders of Connective Tissue the chapter on the mucopolysaccharidoses was entitled "The Hurler Syndrome". Already in 1956, ...
  3. NLM Digital Collections - National Library of Medicine classification : a scheme for the shelf arrangement of library ... 
    Publication: Bethesda, Md. : U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Library of Medicine ; Washington, D.C. : For sale by the Supt. of Docs., U.S. G.P.O., 1994
    resource.nlm.nih.gov/9440818
    ... Metabolism QV 38 Military supplies UH 420-425 Mucopolysaccharidosis IV WD 205.5.C2 Packaging QV 825 ... Arterial Bypass see Cerebral Revascularization Eccentro-Osteochondrodysplasia see Mucopolysaccharidosis IV Eccrine Glands WR 400 ALWAYS CONSULT MAIN ...
  4. NLM Digital Collections - Beikoku Kokuritsu Igaku Toshokan bunruihō : igaku oyobi kanren bun'ya ni okeru tosho haikahō 
    Publication: Tōkyō : Nihon Igaku Toshokan Kyōkai, 1996
    resource.nlm.nih.gov/9704321
    ... Metabolism QV 38 Military supplies UH 420-425 Mucopolysaccharidosis IV WD 205.5.C2 Packaging QV 825 ... Arterial Bypass see Cerebral Revascularization Eccentro-Osteochondrodysplasia see Mucopolysaccharidosis IV Eccrine Glands WR 400 ALWAYS CONSULT MAIN ...
  5. NLM Digital Collections - MEDLARS indexing : integrated authority file 
    Publication: [Bethesda, Md.] : National Library of Medicine, Bibliographic Services Division, 1968
    resource.nlm.nih.gov/0226726
    ... OSTEOPHYTOSIS (68) forme ffuste of Hurler's syndrome see mucopolysaccharidosis V formimino transferase deficiency syndrome an hereditary impairment ... ENAMEL *anatomy 6c histology (68) Hunter's syndrome see mucopolysaccharidosis II Hurler's disease syn. Hurler's syndrome (Ruhl 6c ...
  6. NLM Digital Collections - On Lumpers and Splitters, or the Nosology of Genetic Disease 
    Publication: The National Foundation-March of Dimes, January 1969
    resource.nlm.nih.gov/101584632X94
    ... the focus, eg in studies of the genetic mucopolysaccharidoses and the separation of homocystinuria from the Marfan ... of urinary excretion of mucopoly- saccharides in the mucopolysaccharidoses helps disting- uish several types,2 eg types ...
  7. NLM Digital Collections - Integrated authority file : IAF 
    Publication: [Bethesda, Md.] : U.S. Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health, 1974
    resource.nlm.nih.gov/8909143
    ... marmot X SQUIRRELS Maroteaux-Lamy syndrome (1) X MUCOPOLYSACCHARIDOSIS X CKONDROlTIN/metabolisa p SYNDROKE Maroteaux-Laay syndroae ( ... see Phlebotomus fever virus Sanfilippo's syndrome (SYN) X MUCOPOLYSACCHARIDOSIS X BENTAL RETARDATION P SYNDROHE Sango fever (HSH) ...
  8. NLM Digital Collections - Letter from Robert L. Kaufman to Victor A. McKusick 
    Publication: Produced: 8 April 1971
    resource.nlm.nih.gov/101584632X3
    ... show that the patient probably has a new mucopolysaccharidosis, rather than Sanfilippo's syndrome. This is a patient ... who in addition to x- ray changes of mucopolysaccharidosis and severe neurological problems and retardation, shows chondroitin ...
  9. NLM Digital Collections - Rare diseases. Although limited, available evidence suggests medical and other costs can be ... 
    Publication: Washington, DC : United States Government Accountability Office, October 2021
    resource.nlm.nih.gov/9918383083506676
    ... the Diagnostic Delay in Two Ultra-Orphan Diseases (Mucopolysaccharidosis Types I and III): Potential Causes and Implications," ... is most common in Native American Navajos. 16 Mucopolysaccharidosis refers to a group of inherited conditions in ...
  10. NLM Digital Collections - Proposal for a Genetics Research Center 
    Publication: Produced: 1 June 1973
    resource.nlm.nih.gov/101584906X17932
    ... the clinic where most of the patients with mucopolysaccharidoses, mucolipidoses, simply inherited disorders of bone, Down's syndrome ... A Chemical Method for the Antenatal Diagnosis of Mucopolysaccharidoses." Lancet, 1, 83 (1970). 26c) Nadlec, H. L., ...
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