Congenital Glycosylation Disorder Type 1A (Jacquin Syndrome) in Two Siblings: Case Report

M. S. Rudneva; A. S. Miloserdova

Congenital Glycosylation Disorder Type 1A (Jacquin Syndrome) in Two Siblings: Case Report

M. S. Rudneva, A. S. Miloserdova

Full Text:

PDF (Rus)

Generate QR code

About the Authors
Cited By
Scopus Cited

About the Authors

M. S. Rudneva

Pirogov Russian National Research Medical University
Russian Federation

Maria S. Rudneva,

Moscow

A. S. Miloserdova

Pirogov Russian National Research Medical University
Russian Federation

Anastasia S. Miloserdova,

Moscow

Review

For citations:

Rudneva M.S., Miloserdova A.S. Congenital Glycosylation Disorder Type 1A (Jacquin Syndrome) in Two Siblings: Case Report. Russian Pediatric Journal. 2025;6(4):175. (In Russ.)

JATS XML

This work is licensed under a Attribution-NonCommercial-NoDerivatives 4.0 International.

ISSN 2687-0843 (Online)

Username
Password
	Remember me
Not a user? Register with this site Forgot your password?

User

Russian Pediatric Journal

Congenital Glycosylation Disorder Type 1A (Jacquin Syndrome) in Two Siblings: Case Report

Full Text:

About the Authors

Review

For citations:

Cookies policy