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Shone's complex, Shone's anomaly, or Shone's disease: Specialty: Cardiology: Shone's syndrome is a rare congenital heart defect described by Shone in 1963.
A number of genetic conditions are associated with heart defects, including Down syndrome, Turner syndrome, and Marfan syndrome. [3] Congenital heart defects are divided into two main groups: cyanotic heart defects and non-cyanotic heart defects, depending on whether the child has the potential to turn bluish in color. [3]
An extremely rare complication, it affects 1 in every 40,000 deliveries, and occurs during delivery or shortly after giving birth, when amniotic fluid enters a mother's bloodstream just before ...
Crandall syndrome; Craniosynostosis–anal anomalies–porokeratosis syndrome; Cranio-lenticulo-sutural dysplasia; CREST syndrome; Cri du chat; Crigler–Najjar syndrome; Crome syndrome; Cronkhite–Canada syndrome; Cross syndrome; Crouzon syndrome; Crouzonodermoskeletal syndrome; Crush syndrome; Cruveilhier-Baumgarten syndrome; Cryopyrin ...
According to the Mayo Clinic, Bell's palsy causes weakness in muscles in one side of the face and is often a short-term condition that ultimately improves.. Thomas' revelation comes months after ...
Asymmetric crying facies (ACF), also called partial unilateral facial paresis and hypoplasia of depressor angula oris muscle, [1] is a minor congenital anomaly caused by agenesis or hypoplasia of the depressor anguli oris muscle, one of the muscles that control the movements of the lower lip. This unilateral facial weakness is first noticed ...
ICF syndrome patients exhibit facial anomalies which include hypertelorism, low-set ears, epicanthal folds and macroglossia. [3] Other frequent symptoms observed in individuals with ICF syndrome include intellectual disability, recurrent and prolonged respiratory infections, and integumentary and digestive system infections. [4]
A baby Jesus figurine was returned to a Colorado nativity scene where it was stolen from just days before Christmas — and an apology note was left behind.