{"id":11639,"date":"2025-07-26T08:56:28","date_gmt":"2025-07-26T06:56:28","guid":{"rendered":"https:\/\/valintermed.com\/?p=11639"},"modified":"2025-07-26T08:56:28","modified_gmt":"2025-07-26T06:56:28","slug":"sindrom-hartsfilda","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/hartsfield-syndrome\/","title":{"rendered":"Hartsfield syndrome"},"content":{"rendered":"
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Hartsfield syndrome is a rare genetic disorder characterized by abnormal lung development and respiratory disorders. The main pathogenetic mechanism of this syndrome is a mutation in the genes responsible for the development of lung tissue and the formation of the alveolar structure. As a rule, the disease manifests itself in childhood with severe respiratory failure, and may also be accompanied by other systemic anomalies, including cranial anomalies, cardiovascular diseases, and limb development disorders. Hartsfield syndrome belongs to a group of multisystem disorders and requires a thorough approach to diagnosis and treatment, given its complex genetic background and the diversity of clinical manifestations.<\/p>\n

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