Di George syndrome: Not always a pediatric diagnosis;Sindrome di Di George: Una diagnosi non sempre pediatrica

Recenti Progressi in Medicina

Volumn 104, Issue 2, 2013, Pages 69-

  Bertola, Giorgio ^a   Giambona, Salvatore ^a   Bianchi, Roberto ^a   Girola, Andrea ^a   Berra, Sergio Antonio ^a  

^a RHO HOSPITAL   (Italy)

Author keywords

Di George syndrome

Indexed keywords

ADULT; ARTICLE; BRAIN CALCIFICATION; CASE REPORT; CHROMOSOME DELETION 22Q11; DELAYED DIAGNOSIS; DIGEORGE SYNDROME; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPOCALCEMIA; LYMPHOCYTOPENIA;

ABNORMALITIES, MULTIPLE; BRAIN DISEASES, METABOLIC; CALCINOSIS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DELAYED DIAGNOSIS; DIGEORGE SYNDROME; EPILEPSY; FEMALE; HETEROZYGOTE; HUMANS; HYPOCALCEMIA; HYPOPARATHYROIDISM; INTELLECTUAL DISABILITY; MIDDLE AGED; PSYCHOTIC DISORDERS;

EID: 84876584542     PISSN: 00341193     EISSN: 20381840     Source Type: Journal    
DOI: 10.1701/1241.13707     Document Type: Article

References (4)

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4. Johnston PC, Donnelly DK, Morrison PJ, Hunter SJ. Di George syndrome presenting as late onset hypocalcaemia in adulthood. Ulster Med J 2008; 77: 201-2.