Clinical difficulties of diagnostics of a syndrome of Prader–Willi

Abstract


Prader–Willi’s syndrome is a genetic anomaly which often masks under cerebral spastic infantile paralysis and myopathy diagnoses. Though at careful collecting the anamnesis, attentive survey of the patient and competent genetic inspection the diagnosis usually doesn’t raise doubts.

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About the authors

Valentina Ivanovna Guzeva

Saint-Petersburg State Pediatric Medical University

Email: viktoryra@mail.ru
Dr Med Sci., Professor, Head of Department of nervous diseases

Lyubov Borisovna Bessonova

Saint Olga Children city hospital N 4

Email: yuba-bessonova@mail.ru
MD, Head, Neurologic Dept.

Kristina Arturovna Seel

Saint-Petersburg State Pediatric Medical University

Email: kristina_seel@list.ru
Student

References

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  4. Тейлор Р. Б. Трудный Диагноз. Том 2. — М.: «Медицина». — 1992. — С. 338. Clinical difficulties of diagnostics of a syndrome of Prader–Willi

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Copyright (c) 2013 Guzeva V.I., Bessonova L.B., Seel K.A.

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