Novel prenatally diagnosed compound heterozygous POMT2 variants in fetal congenital primary aqueduct stenosis
Objective: To study the etiology of congenital hydrocephalus in genetic aqueduct stenosis. Case report: We report the case of a 31-year-old pregnant female, G2P0A1, with a history of hyperthyroidism under medical control. The patient received regular prenatal care, with no specific findings in the L...
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| Автори: | , , , , , |
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| Формат: | Книга |
| Опубліковано: |
Elsevier,
2022-05-01T00:00:00Z.
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| Онлайн доступ: | Connect to this object online. |
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Connect to this object online.3rd Floor Main Library
| Шифр: |
A1234.567 |
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| Примірник 1 | Доступно |