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Congenital multiple pituitary hormone deficiency associated with hyperammonemia: a case report with a short review of the literature
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نویسنده
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Inoue H ,Ihara K ,Ochiai M ,Takahata Y ,Kohno H ,Hara T
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منبع
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journal of perinatology - 2011 - دوره : 31 - شماره : 2 - صفحه:146 -148
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چکیده
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We herein report a case study of a female newborn with multiple pituitary hormone deficiencies who presented with generalized seizures, hypoglycemia and hyperammonemia at 18 h after birth. in addition, we review the association of hyperammonemia in neonates with multiple pituitary hormone deficiencies reported in the previous literature. this unrecognized association should be taken into account for the early diagnosis and treatment of these patients.
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آدرس
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Kyushu University, Department of Pediatrics, Japan, Kyushu University, Department of Pediatrics, Japan, Kyushu University, Department of Pediatrics, Japan, Kyushu University, Department of Pediatrics, Japan, Fukuoka Chlidren's Hospital, Department of Endocrinology and Metabolism, Japan, Kyushu University, Department of Pediatrics, Japan
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Authors
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