Family case of legg-calve-perthes disease
DOI:
https://doi.org/10.15574/PS.2019.63.104Keywords:
The Legg-Calve-Perthes disease, heredity, research, treatmentAbstract
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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