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  • Clinical case of Pierre Robin’s syndrome in a newborn child

    Редакция | 2013, PM Pediatrics. Clinical observations, Practical medicine 06 (13) Pediatrics | 25 ноября, 2013

    L.F. VAKHITOVA, L.K. PHAZLEEVA, L.G. BULGAKOVA, O.V. VARLAMOVA
    Kazan State Medical University
    Children’s Republican Clinical Hospital of the Ministry of Health of the Republic of Tatarstan, Kazan

    Vakhitova Liliya Phaukatovna
    Candidate of Medical Science, Assistant Professor of Hospital Pediatrics
    49 Butlerova Str., Kazan 420012
    Tel. (843) 237-30-37, e-mail: [email protected]

    Early diagnosis of congenital abnormal development currently remains relevant because of the increasing frequency of this disease and the need for measures aimed at preventing possible complications. This article describes a rare case of clinically apparent severe Pierre Robin’s syndrome in a newborn child.

    Key words: newborn, hereditary syndromes, Pierre Robin’s syndrome.

     

    REFERENCES

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    10. Tolarova M., Senders C. Medicine, Pierre Robin Malformation. — Last updated June 2006.

    11. Wagener S., Rayatt S.S., Tatman A.J. et al. Management of infants with Pierre Robin sequence // Cleft Palate Craniofac J. — 2003 Mar. — Vol. 40, № 2. — P. 180-185.

    12. Kirillova L.G., Tkachuk L.I., Shevchenko A.A., Silaeva L.Ju., Lisica V.V., Mironjak L.A. Sindrom P’era Robena u detej // Mezhdunarodnyj nevrologicheskij zhurnal. — 2010. — № 3.

    Метки: Hereditary syndromes, L.F. Vakhitova, L.G. Bulgakova, L.K. Phazleeva, Newborn, O.V. Varlamova, Pierre Robin’s syndrome, Practical medicine 06 (13) Pediatrics

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