Medicine:Holt–Oram syndrome

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Holt-Oram syndrome
Other namesHeart-hand syndrome, Atrio-digital syndrome, Atriodigital dysplasia
Autosomal dominant - en.svg
Holt-Oram syndrome has an autosomal dominant pattern of inheritance

Holt–Oram syndrome (also called atrio-digital syndrome, atriodigital dysplasia, cardiac-limb syndrome, heart-hand syndrome type 1, HOS, ventriculo-radial syndrome) is an autosomal dominant disorder that affects bones in the arms and hands (the upper limbs) and often causes heart problems.[1] The syndrome may include an absent radial bone in the forearm, an atrial septal defect in the heart, or heart block.[2] It affects approximately 1 in 100,000 people.[2]


All people with Holt-Oram syndrome have, at least one, abnormal wrist bone, which can often only be detected by X-ray.[1] Other bone abnormalities are associated with the syndrome. These vary widely in severity, and include a missing thumb, a thumb that looks like a finger, upper arm bones of unequal length or underdeveloped, partial or complete absence of bones in the forearm, and abnormalities in the collar bone or shoulder blade.[1][2] Bone abnormalities may affect only one side of the body or both sides; if both sides are affected differently, the left side is usually affected more severely.[1]

About 75 percent of individuals with Holt–Oram syndrome also have congenital heart problems,[2] with the most common being defects in the tissue wall between the upper chambers of the heart (atrial septal defect) or the lower chambers of the heart (ventricular septal defect).[3] People with Holt–Oram syndrome may also have cardiac conduction disease, or abnormalities in the electrical system that coordinates contractions of the heart chambers.[1] Cardiac conduction disease can lead to slow heart rate (bradycardia); rapid, ineffective contraction of the heart muscles (fibrillation); and heart block.[1][2] People with Holt-Oram syndrome may have only congenital heart defects, only cardiac conduction disease, both or neither.[1][2]


Mutations in the TBX5 gene cause Holt–Oram syndrome.[1] The TBX5 gene produces a protein that is critical for the proper development of the heart and upper limbs before birth.[1]

Holt–Oram syndrome has an autosomal dominant pattern of inheritance, meaning one abnormal copy of the gene is sufficient to cause disease, which each child has a 50% chance of inheriting from an affected parent.[1] However, in 85 percent of cases, the gene mutation isn't inherited, but a new mutation.[2]


Diagnosis may be made on physical features alone, if a person has an arm or hand bone abnormality and a personal or family history of heart problems.[2] If the symptoms aren't enough to diagnose, a person may undergo genetic testing for the mutations associated with the syndrome.[2]


A person with Holt-Oram syndrome may need various treatments, depending on how the syndrome manifests. Surgery, prosthetics and physical or occupational therapy can help people with bone abnormalities.[2] Heart defects may call for surgery, medication, pacemakers or close monitoring.[2] Pregnant women with Holt-Oram syndrome and heart abnormalities should be followed by a cardiologist during pregnancy.[2]


It is named for Mary Holt and Samuel Oram, who published a paper on it in 1960.[4][5]

See also

  • Absent radius
  • Heart-hand diseases


  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 "Holt-Oram syndrome". U.S. National Library of Medicine. June 2014. 
  2. 2.00 2.01 2.02 2.03 2.04 2.05 2.06 2.07 2.08 2.09 2.10 2.11 McDermott, Deborah A.; Fong, Jamie C.; Basson, Craig T. (2015-10-08). Adam, MP; Ardinger, HH; Pagon, RA. eds. "Holt-Oram Syndrome". GeneReviews (Seattle, WA: University of Washington). PMID 20301290. Retrieved 2018-01-01. 
  3. Bossert, T; Walther, T; Gummert, J; Hubald, R; Kostelka, M; Mohr, FW (October 2002). "Cardiac malformations associated with the Holt-Oram syndrome—report on a family and review of the literature.". The Thoracic and Cardiovascular Surgeon 50 (5): 312–4. doi:10.1055/s-2002-34573. PMID 12375192. 
  4. Virdis, G.; Dessole, M.; Dessole, S.; Ambrosini, G.; Cosmi, E.; Cherchil, P. L.; Capobianco, G. (2016-01-01). "Holt Oram syndrome: a case report and review of the literature". Clinical and Experimental Obstetrics & Gynecology 43 (1): 137–139. doi:10.12891/ceog3060.2016. ISSN 0390-6663. PMID 27048037. 
  5. Holt, Mary; Oram, Samuel (1960-04-01). "Familial Heart Disease with Skeletal Malformations". British Heart Journal 22 (2): 236–242. doi:10.1136/hrt.22.2.236. ISSN 0007-0769. PMID 14402857. 

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