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PMID: 7170191 Published · ppublish ita English Abstract Journal Article

[Mannosidosis. Study of two families and prenatal diagnosis].

La mannosidosi. Studio di due famiglie e diagnosi prenatale.

La Pediatria medica e chirurgica : Medical and surgical pediatrics ·Vol. 4 ·No. 3 ·1982-00-00 ·Pages 203-14

Cerruti Mainardi P, Gatti R, Javarone A, Filocamo M, Levis F, Borrone C

Abstract

Mannosidosis is a human lysosomal storage disease caused by and acid alpha-mannosidase deficiency. We have studied two affected Italian families and in this paper discuss the problems concerning the clinical and radiological findings, and laboratory assay as an access to diagnosis. Reference is made to our personal experience, as concerns the difficulties of carrier detection and of prenatal diagnosis.

MeSH Terms
Chromatography, Thin Layer Female Humans Hydrogen-Ion Concentration Leukocytes/enzymology Male Mannosidases/deficiency Metabolism, Inborn Errors/diagnosis,genetics Pedigree Pregnancy Prenatal Diagnosis
Chemicals
Mannosidases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Cerruti Mainardi P
Gatti R
Javarone A
Filocamo M
Levis F
Borrone C
Article Info
Journal
La Pediatria medica e chirurgica : Medical and surgical pediatrics
Abbr.
Pediatr Med Chir
ISSN
0391-5387
Published
1982-00-00
Pages
203-14
Language
ita
Region
Italy
NLM ID
8100625
Subset
IM
External Links
PubMed source
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