Search results
Results from the WOW.Com Content Network
Loeys–Dietz syndrome (LDS) is an autosomal dominant genetic connective tissue disorder. It has features similar to Marfan syndrome and Ehlers–Danlos syndrome. [3][4][5] The disorder is marked by aneurysms in the aorta, often in children, and the aorta may also undergo sudden dissection in the weakened layers of the wall of the aorta.
Not known. Familial thoracic aortic aneurysm and aortic dissection is a very rare vascular genetic disorder, it's characterized by recurrent thoracic aortic aneurysms and aortic dissections within a family, these mentioned complications affect one or more aortic segments without any other disease being associated with them.
Joe West [1] Joey + Rory chronology. Country Classics: A Tapestry of Our Musical Heritage. (2014) Hymns That Are Important to Us. (2016) Hymns That Are Important to Us is the eighth and final studio album by Joey + Rory. Gaither Music Group released the album on February 12, 2016. It won the Grammy Award for Best Roots Gospel Album in 2017.
Chronic functional abdominal pain. Chronic infantile neurologic cutaneous and articular syndrome. Chronic Lyme disease. Chronic prostatitis/chronic pelvic pain syndrome. Churg–Strauss syndrome. Chédiak–Higashi syndrome. Claude's syndrome. Clinically isolated syndrome. CLOVES syndrome.
Pectus excavatum is a structural deformity of the anterior thoracic wall in which the sternum and rib cage are shaped abnormally. This produces a caved-in or sunken appearance of the chest. It can either be present at birth or develop after puberty.
Hypertelorism is an abnormally increased distance between two organs or bodily parts, usually referring to an increased distance between the orbits (eyes), or orbital hypertelorism. In this condition the distance between the inner eye corners as well as the distance between the pupils is greater than normal. Hypertelorism should not be confused ...
Frequency. 1 in 5,000 [1] Ehlers–Danlos syndromes (EDS) are a group of 13 genetic connective-tissue disorders. [7] Symptoms often include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. [1] These may be noticed at birth or in early childhood. [3]
Genetic mutations. Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder of the nervous system which prevents the feeling of pain or temperature and prevents a person from sweating. Cognitive disorders are commonly coincidental. CIPA is the fourth type of hereditary sensory and autonomic neuropathy (HSAN ...