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O que (quem) é DiGeorge syndrome - definição
DiGeorge syndrome
![Result of FISH analysis using LSI probe (TUPLE 1) from DiGeorge/velocardiofacial syndrome critical region. TUPLE 1 ([[HIRA]]) probe was labeled in Spectrum Orange and [[Arylsulfatase A]] (ARSA) in Spectrum Green as control. Absence of the orange signal indicates deletion of the TUPLE 1 locus at 22q11.2.](https://commons.wikimedia.org/wiki/Special:FilePath/Fish analysis di george syndrome.jpg?width=200 "Result of FISH analysis using LSI probe (TUPLE 1) from DiGeorge/velocardiofacial syndrome critical region. TUPLE 1 ([[HIRA]]) probe was labeled in Spectrum Orange and [[Arylsulfatase A]] (ARSA) in Spectrum Green as control. Absence of the orange signal indicates deletion of the TUPLE 1 locus at 22q11.2.")
T CELL DEFICIENCY DISEASE THAT IS THE RESULT OF A LARGE DELETION OF CHROMOSOME 22, WHICH INCLUDES THE DGS GENE NEEDED FOR DEVELOPMENT OF THE THYMUS AND RELATED GLANDS WITH SUBSEQUENT LACK OF T-CELL PRODUCTION
Di George's syndrome; Chromosome 22, microdeletion 22 q11; VCFS; Velocardio-facial syndrome (VCFS); Unusual face syndrome; Shprintzen syndrome; Craniofacial syndrome; Conotruncal face anomaly; Di George syndrome; Velocardio-facial syndrome; CATCH 22 syndrome; Velocardiofacial syndrome; 22q; Digeorge's syndrome; Digeorge syndrome; DiGeorge Syndrome; Autosomal dominant opitz G/BBB syndrome; Caylor cardiofacial syndrome; Conotruncal anomaly face syndrome; Chromosome 22 deletion syndrome; Thymic aplasia; DiGeorge's syndrome; DiGeorge's Syndrome; 22q11.2; Velo-cardio-facial syndrome; 22q11 deletion; Di George Syndrome; Digeorge; Velo cardio facial syndrome; Velocardiofacial Syndrome; Velo-cardio-facial Syndrome; Strong Syndrome; Shprintzen's syndrome; DiGeorge anomaly; Chromosome 22q11 deletion; DiGeorge; 22q11 deletion syndrome; Velocariofacial syndrome; Velocardiofacial; Craniofacial syndromes; Chromosome 22q11.2 deletion syndrome, distal; 22q11.2 deletion syndrome; Digeorge syndrome chromosome region
velocardiofacial syndrome (VCFS), Shprintzen syndrome, conotruncal anomaly face syndrome (CTAF), Takao syndrome, Sedlackova syndrome, Cayler cardiofacial syndrome, CATCH22, 22q11.2 deletion syndrome
Reye's syndrome
SYNDROME CHARACTERIZED BY ACUTE BRAIN DAMAGE AND LIVER FUNCTION PROBLEMS
Reyes Syndrome; Reye Syndrome; Reye's Syndrome; Reyes syndrome; Reye’s Syndrome; Reye hepatocerebral syndrome; Rye syndrome; Reye s syndrome; Reye's s syndrome; Reye's syndrome; Reye’s syndrome
['re?z, 'r??z]
¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.
Origin
1960s: named after the Australian paediatrician Ralph D. K. Reye.
Frey's syndrome
HUMAN DISEASE
Auriculotemporal syndrome; Frey syndrome
Frey's syndrome (also known as Baillarger's syndrome, Dupuy's syndrome, auriculotemporal syndrome, or Frey-Baillarger syndrome) is a rare neurological disorder resulting from damage to or near the parotid glands responsible for making saliva, and from damage to the auriculotemporal nerve often from surgery.
