Isolated Partial Gowth Hormone Deficient Short Stature with Syringomyelia not Associated with Birth Injury

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概要

• 論文の詳細を見る

• A 59-year-old female with 20-year history of slowly progressing muscle atrophy and sensory disturbance of upper extremities showed short stature, scoliosis, hunger type of sensory dissociation of the upper extremities and pyramidal tract sign of the lower extremities. Magnetic resonance imaging (MRI) clarified hypoplasia of the anterior pituitary lobe, Arnold-Chiari malformation and cervical syringomyelia. Insulin and arginine stimulating tests revealed partial type of isolated growth hormone (GH) deficiency but GH gene analysis detected no defects of GH genes. It was considered to be a rare case of non-hereditary hypopituitarism with Chiari malformation and syringomyelia not associated with perinatal injury, namely a midline anomaly syndrome.(Internal Medicine 37: 674-677, 1998)

• 社団法人 日本内科学会の論文
• 1998-08-01

著者

• Koga Tomoyuki

  The Department Of Neurology Otemachi Hospital (at Time Of Study) Present Addressis The Department Of

• Otsuka Takako

  The Department Of Child Development Kumamoto University School Of Medicine

• ABE Tomoko

  the Third Department of Internal Medicine, Oita Medical School

• NORIYUKI Hideki

  the Department of Neurology, Otemachi Hospital (at time of study), present addressis the Department

• IWATANI Noritaka

  the Department of Child Development, Kumamoto University School of Medicine

• Iwatani Noritaka

  The Department Of Child Development Kumamoto University School Of Medicine

• Noriyuki Hideki

  The Department Of Neurology Otemachi Hospital (at Time Of Study) Present Addressis The Department Of

• Abe Tomoko

  The Third Department Of Internal Medicine Oita Medical School

関連論文

• Isolated Partial Gowth Hormone Deficient Short Stature with Syringomyelia not Associated with Birth Injury

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