Ad
related to: holt oram syndrome cardiac manifestations- What Is HCM?
Learn More About HCM
On The Patient Website
- HCM Diagnosis
The Path To An HCM Diagnosis Can
Be Challenging. Learn More.
- HCM Treatment Options
Management Strategies
For Symptomatic Obstructive HCM
- HCM Support And Resources
Hear From People
Living With HCM
- What Is HCM?
Search results
Results From The WOW.Com Content Network
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]
Heart-hand syndromes are a group of rare diseases that manifest with both heart and limb deformities. [1] [2] [3] [4]As of July 2013, known heart-hand syndromes include Holt–Oram syndrome, Berk–Tabatznik syndrome, brachydactyly-long thumb syndrome, patent ductus arteriosus-bicuspid aortic valve syndrome, heart hand syndrome, Slovenian type and Heart-hand syndrome, Spanish type.
Ho–Kaufman–Mcalister syndrome: Holt–Oram syndrome: ASD, and a first degree heart block. Hypoplastic left heart syndrome: Jacobsen syndrome: genetic (Chromosome 11q deletion) Jaffe–Campanacci syndrome: Jervell and Lange-Nielsen syndrome: genetic (autosomal recessive) a type of long QT syndrome: Kabuki syndrome: Kearns–Sayre syndrome ...
[23] [10] Holt-Oram syndrome can cause a hole in the septum, [9] bone abnormalities in the fingers, wrists, or arms, [24] and a conduction disease leading to abnormal heart rates and arrhythmias. [8] The most common cardiac issue associated with this condition is the malformation of the septum, which separates the left and right sides of the heart.
Mutations of all these proteins are associated with both atrial and ventricular septal defects; In addition, NKX2-5 is associated with defects in the electrical conduction of the heart and TBX5 is related to the Holt–Oram syndrome which includes electrical conduction defects and abnormalities of the upper limb.
Familial opposable triphalangeal thumb duplication is a limb malformation syndrome and a type of pre-axial polydactyly, characterized by having duplicated opposable triphalangeal thumbs. This condition can be a symptom of other genetic disorders, such as Holt–Oram syndrome and Fanconi anemia.
Hereditary leiomyomatosis and renal cell cancer syndrome; Hereditary neuralgic amyotrophy; Hereditary nonpolyposis colorectal cancer; Hermansky–Pudlak syndrome; Hero syndrome; Heyde's syndrome; High-rise syndrome; HIV/AIDS; Holiday heart syndrome; Holt–Oram syndrome; Horn-Kolb syndrome; Horner's syndrome; Howel–Evans syndrome; Hoyeraal ...
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...