Family case of legg-calve-perthes disease

Authors

  • M. D. Protsailo I. Horbachevsky Ternopil State Medical University, Ukraine, Ukraine
  • I. O. Kryckyy I. Horbachevsky Ternopil State Medical University, Ukraine, Ukraine

DOI:

https://doi.org/10.15574/PS.2019.63.104

Keywords:

The Legg-Calve-Perthes disease, heredity, research, treatment

Abstract

The Legg-Calve-Perthes disease (LCPD) is a serious disease that has a hidden beginning, which gives rise to a frivolous attitude towards it of both medical

professionals and parents

The absence of pain syndrome, the eradicated clinical picture distort the true picture of this ailment, so there were a few false postulates (myths) regarding

etiology, early diagnosis, treatment and pros.

Our clinical observation is interesting because, against the background of familial congenital connective tissue dysplasia, the mother and her two children

(a boy and a girl) were diagnosed with left-sided LCPD.

An analysis of recent data on genetics, breeding, orthopedics, biochemistry, cardiology and other sciences has shown that LCPD is a separate manifestation

of more general lesions of the connective tissue of the whole organism, which has hereditary predility – a syndrome of congenital dysplasia that connects

the tissue. In English literature, he is referred to as MASS- syndrome. Thanks to this data, the main ones have been refuted.

The system of defeat at LCPD, the latent course of the disease, severe complications, high disability, significant differences in the severity of etiology, diagnosis,

treatment, and prophylaxis indicate that it is an important medical and social problem.

Conclusions 1. Diagnostics of LCPD is rather conditional, treatment begins with delay. 2. LCPD is tend to genetic transmission. 3. This is a separate syndrome

of the whole organism MASS syndrome.

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