Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes. [electronic resource]
Producer: 19990330Description: 678-83 p. digitalISSN:- 1098-4275
- Amniotic Fluid -- cytology
- Bartter Syndrome -- diagnosis
- DNA Mutational Analysis
- Female
- Humans
- Indomethacin -- therapeutic use
- Infant, Newborn
- Kidney -- diagnostic imaging
- Male
- Polyhydramnios -- drug therapy
- Polymorphism, Single-Stranded Conformational
- Potassium Channels
- Pregnancy
- Prenatal Diagnosis
- Prostaglandins E -- blood
- Syndrome
- Ultrasonography
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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