What is Holt-Oram syndrome?
Holt-Oram syndrome is characterized by skeletal abnormalities of the hands and arms (upper limbs) and heart problems.
Holt-Oram syndrome is dominant (requires only one copy in the genome to be expressed) and is often associated with skeletal deformities such as abnormally short forearms or thumbs.
Inheritance: autosomal dominant.
Holt-Oram syndrome: A genetic syndrome characterized by the combination of heart disease and malformations of the upper limb.
Holt-Oram syndrome is a disorder that is characterized by abnormalities in the bones of the upper limb and a family or personal history of a congenital heart malformation or an abnormality in the electrical impulses that coordinate the muscle ...
Holt-Oram syndrome, also known as hand-heart syndrome, an inherited disorder that causes malformations in the heart and upper limbs ...
It is seen in the autosomal recessive Baller-Gerold syndrome and Holt-Oram syndrome, an autosomal dominant condition that sometimes involves amelia.
Health Opinion Survey; High-order Spectrum; Holt-Oram Syndrome; Human Osteosarcoma; Hypoosmotic Swelling [test]
HRC
Health Reference Center; Hereditary Renal Cancer; High-resolution Chromatography; Horse Red Cell; Human Rights Committee ...
ears, eyes, kidneys and nervous system and as a component of Okihiro syndrome (an association of Duane syndrome with forearm malformation and hearing loss), Wildervanck syndrome (fusion of neck vertebrae and hearing loss), Holt-Oram syndrome ...
Holt-Oram syndrome
Homozygous Beta Thalassaemia see Thalassaemia Major (ß Thalassaemia)
HOOD see Nail-Patella syndrome
Horner syndrome see Erb's Palsy
HPE see Holoprosencephaly
HPRT deficiency see Lesch Nyhan syndrome
HPRT see Lesch Nyhan syndrome ...
 See also: Autosomal dominant, Symptom, Kidney, Dysplasia, Depression
  
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