Autor: |
Weissbach, T., Moran, H., Yanay, Z., Massarwa, A., Meyer, R., Leibovitch, L., Berkenstadt, M., Weisz, B., Mazaki‐Tovi, S., Kassif, E. |
Zdroj: |
Ultrasound in Obstetrics & Gynecology; Sep2022 Supplement S1, Vol. 60, p213-213, 1p |
Abstrakt: |
Comprehensive genetic testing is the cornerstone of diagnosis of hypotonic conditions and should be considered when 1 overt sign or 2 subtle/nonspecific signs are present. Describe prenatal sonographic signs of marked congenital hypotonia and propose a diagnostic flowchart. Fetal hypotonia was defined as sonographic signs suggestive of hypotonia, with or without a genetic causality. [Extracted from the article] |
Databáze: |
Complementary Index |
Externí odkaz: |
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