Velo cardio facial syndrome symptoms

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DiGeorge syndrome, more accurately known by a broader term — 22q This deletion results in the poor development of several body systems. The term 22q

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What is a 22q Each chromosome is made of protein and deoxyribonucleic acid DNA. Passed from parents to offspring, DNA contains the specific instructions that make each type of living creature unique.

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What is 22q11 DS? People with 22q11 are missing a small piece from chromosome Calcium: Children with 22q Deletion Syndrome may have decreased calcium levels.

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DiGeorge syndrome, more accurately known as 22q The condition is also known by several other names, including velocardiofacial syndrome, Shprintzen syndrome, and conotruncal anomaly face syndrome. People with 22q11 DS can have a wide variety of medical conditions, including heart defects, cleft palate, speech or feeding problems, difficulty fighting infections, low calcium levels, kidney problems, learning or behavioral issues, and unique facial features. Children with 22q11 DS can have a wide range of signs and symptoms, with differing degrees of severity.

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DiGeorge syndrome is a chromosomal disorder that typically affects the 22nd chromosome. Several body systems develop poorly, and there may be medical problems, ranging from a heart defect to behavioral problems and a cleft palate. The condition is also known as 22q

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Velocardiofacial syndrome, or 22q11 deletion syndrome, is known by many names, including Shprintzen syndrome, craniofacial syndrome, DiGeorge syndrome, or conotruncal anomaly face syndrome. VCFS includes many common features: cleft palate, heart defects and a characteristic facial appearance. Other common findings include minor learning problems and speech and feeding problems.

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Velocardiofacial syndrome, or VCFS, is a complex syndrome that has been associated with more than 30 different characteristics, including defects of the palate, heart defects, learning disabilities and distinct facial features. The severity of VCFS and the characteristics that appear vary widely between individuals. It's inherited in an autosomal dominant fashion, meaning if one parent has the syndrome, each child has a 50 percent chance of inheriting it.

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Velocardiofacial syndrome VCFS is a genetic condition that is sometimes hereditary. VCFS is characterized by a combination of medical problems that vary from child to child. These medical problems include: cleft palate, or an opening in the roof of the mouth, and other differences in the palate; heart defects; problems fighting infection; low calcium levels; differences in the way the kidneys are formed or work; a characteristic facial appearance; learning problems; and speech and feeding problems.

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What is 22q The 22q In children with this syndrome, a tiny piece of chromosome 22 is missing. This can cause many health problems.

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