{"id":12599,"date":"2024-10-11T18:55:02","date_gmt":"2024-10-11T16:55:02","guid":{"rendered":"https:\/\/valintermed.com\/?p=12599"},"modified":"2024-10-11T18:55:02","modified_gmt":"2024-10-11T16:55:02","slug":"posledovatelnost-pera-robina","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sequentiality-of-the-robins\/","title":{"rendered":"Pierre Robin's Sequence"},"content":{"rendered":"
<\/div>\n

Pierre Robin sequence (PSRP) is a congenital syndrome characterized by a characteristic combination of features including microcephaly, micrognathia, cleft lip (or palate), and abnormalities in the position and development of the ears. These changes occur as a result of developmental abnormalities during embryogenesis, which consist of insufficient migration of cells and structures responsible for the formation of the maxillofacial region. PSRP can sometimes be accompanied by respiratory and feeding problems related to the narrowness of the airways, which significantly affects the quality of life of patients. The syndrome most often affects girls, and its diagnosis is often made at the neonatal level or in early childhood. It is important to consider that Pierre Robin is part of a wider spectrum of disorders, including clusters of conditions associated with isolated and combined developmental anomalies.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n