英: hypomorph
関: ハイ・モルフ

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 鎌状赤血球形質sickle cell trait [show details]
… disease and sickle cell trait. All states in the United States have been mandated to offer testing since 2006, and the proportion of parents opting out of screening is extremely low . However, the reporting …
2. 外傷性前房出血：臨床的特徴および診断traumatic hyphema clinical features and diagnosis [show details]
… reduced the number of patients with sickle cell disease, notification of sickle cell trait after neonatal screening may be as low as 50 percent in some regions. Patients with suspected or known bleeding dyscrasia …
3. ヘモグロビン変異の概要introduction to hemoglobin mutations [show details]
…has clinical implications. Differences in rates of assembly explain not only the low proportion of HbS in sickle cell trait (35 to 45 percent HbS) but also why the proportion of HbS in SC red cells is 10 …
4. 12歳未満の小児の鉄欠乏症：スクリーニング、予防、臨床症状、診断iron deficiency in infants and children less than12 years screening prevention clinical manifestations and diagnosis [show details]
… reticulocytes, and low values reliably indicate early iron deficient erythropoiesis, prior to onset of anemia . However, the CHr/Ret-He is also low in patients with thalassemia trait. Other conditions …
5. 見かけの鉱質コルチコイド過剰（AME）症候群（長期甘草摂取を含む）apparent mineralocorticoid excess syndromes including chronic licorice ingestion [show details]
… severe juvenile hypertension that is usually transmitted as an autosomal recessive trait . AME is characterized by low birth weight, failure to thrive, onset of severe hypertension in early childhood with …

Related Links

先天性側弯症における TBX6 のヌル多様体と共通して認められる ...

January 22, 2015 Vol. 372 No. 4 先天性側弯症における TBX6 のヌル多様体と共通して認められる低形質アレル TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis N. Wu and Others 前へ次へ