Noonan Syndrome Presenting Growth Hormone Neurosecretory Dysfunction.
スポンサーリンク
概要
- 論文の詳細を見る
Noonan syndrome has been diagnosed by the characteristic physical stigmata for more than two decades. Recent studies of growth hormone secretory pattern provide a new category of growth hormone neurosecretory dysfunction to characterize short stature. We describe herein a case of growth hormone neurosecretory dysfunction in a 16-year-old boy with Noonan syndrome. Growth hormone neurosecretory dysfunction was diagnosed primarily based on the low amplitude and small numbers of the spontaneous bursts of growth hormone secretion during 12-hour nocturnal growth hormone sampling. Treatment with synthetic human growth hormone has markedly accelerated the growth velocity for one year and a half. This case notes the wide spectrum of short stature in Noonan syndrome and the effectiveness of treatment with human growth hormone.(Internal Medicine 31 : 908-911, 1992)
- 社団法人 日本内科学会の論文
著者
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Takemura Yoshihiro
The Department Of Medicine School Of Medicine Dokkyo University Koshigaya Hospital
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Sato Akira
The Department Of Medicine Koshigaya Hospital Dokkyo University School Of Medicine
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TANAKA Katsuya
the Department of Internal Medicine, Koshigaya Hospital, Dokkyo University School of Medicine
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NAITO Takeshi
the Department of Internal Medicine, Koshigaya Hospital, Dokkyo University School of Medicine
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KURAMOCHI Kimihiro
the Department of Internal Medicine, Koshigaya Hospital, Dokkyo University School of Medicine
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ITABASHI Hideo
the Department of Internal Medicine, Koshigaya Hospital, Dokkyo University School of Medicine
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TAKEMURA Yoshihiro
the Department of Internal Medicine, Koshigaya Hospital, Dokkyo University School of Medicine
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- Noonan Syndrome Presenting Growth Hormone Neurosecretory Dysfunction.