小儿手-心畸形综合征 - 百度百科
小儿手-心畸形综合征即心血管-肢体综合征，又称霍-奥（Holt-Oram）综合征、心房-手指综合征、上肢心血管综合病征、家族性心脏和上肢缺陷、心房指趾发育不全、心房及指发育不良综合征等，发病率约1/100000。
Holt-Oram Syndrome - StatPearls - NCBI Bookshelf
2023年8月14日 · Holt-Oram syndrome also referred to as the heart-hand syndrome, is an autosomal dominant disorder that is distinguished by upper limb abnormalities in association with congenital heart lesions. All patients and family members should receive genetic counseling from a qualified clinician.
Holt-Oram综合征（小儿手-心畸形综合征） - 心血管 - 天山医学院
英文：Holt-Oram syndrome, HOS; 同义名：心-手综合征、小儿手-心畸形综合征、心房-指综合征、心肢综合征、心房-手指发育不良、上肢血管综合征、家族性心脏上肢异常综合征、遗传性心血管-上肢畸形综合征。
Holt-Oram Syndrome | Circulation - AHA/ASA Journals
1999年3月16日 · The Holt-Oram syndrome is an autosomal dominant heritable disorder characterized by skeletal upper-limb dysplasias and congenital cardiac defects. We describe a 43-year-old woman who presented with paroxysmal tachycardia and progressive heart failure.
HOLT-ORAM氏症候群 - 百度百科
holt-oram氏症候群是一种不常见的症候群，但在全世界各个不同族群中却都有个案被报告出来。此症的发生没有特别的性别差异，男性跟女性都有可能发生；产前的超音波检查或许可以侦测到一些比较严重的肢体畸形。
Entry - #142900 - HOLT-ORAM SYNDROME; HOS - OMIM
Moens, P., De Smet, L., Fabry, G., Fryns, J. P. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestation in a four generation family. Genet. Counsel. 4: 277-280, 1993.
Holt-Oram Syndrome - Cleveland Clinic
What is Holt-Oram syndrome? Holt-Oram syndrome is a rare, congenital (present at birth) disorder. It often involves abnormal bones in your hands, wrists and arms, as well as heart problems.
Holt-Oram Syndrome Clinical Presentation - Medscape
Holt-Oram syndrome, also called heart-hand syndrome, is an inherited disorder characterized by abnormalities of the upper limbs and heart. Holt and Oram first described this condition in 1960...
Orphanet: Holt-Oram syndrome
A genetic syndrome with limb reduction defects characterized by skeletal abnormalities of the upper limbs and mild-to-severe congenital cardiac defects.
Holt-Oram Syndrome - GeneReviews® - NCBI Bookshelf
2004年7月20日 · To establish the extent of disease and needs in an individual diagnosed with Holt-Oram syndrome (HOS), the evaluations summarized in Table 3 (if not performed as part of the evaluation that led to the diagnosis) are recommended.
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