Множественная эпифизарная дисплазия у детей (клинические проявления, диагностика, лечение)
Диссертация
Пациентам с установленным диагнозом МЭД целесообразно биохимическое исследование уровня ХОМБ в плазме крови с целью контроля течения заболевания и выявления пациентов с возможной мутацией гена COMP (предельно низкие уровни ХОМБ могут свидетельствовать о мутации в гене COMP или задержки роста матриксаповышение показателя ХОМБ — об активном дистрофическом процессе хрящевого матрикса или об активном… Читать ещё >
Список литературы
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