Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

The Journal of Pediatrics

Volumn 109, Issue 3, 1986, Pages 489-492

  Greenberg, Frank ^a   Valdes, Cecilia ^a   Rosenblatt, Howard M ^a   Kirkland, John L ^a   Ledbetter, David H ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RADIOISOTOPE;

CASE REPORT; CHROMOSOME 10P; CHROMOSOME DELETION 10; CONGENITAL DISORDER; CONGENITAL MALFORMATION; ENDOCRINE SYSTEM; HEREDITY; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; PARTIAL MONOSOMY 10; PATIENT; PRESCHOOL CHILD; PRIORITY JOURNAL; T LYMPHOCYTE;

CHILD, PRESCHOOL; CHROMOSOME DELETION; FEMALE; HUMANS; HYPOPARATHYROIDISM; IMMUNOLOGIC DEFICIENCY SYNDROMES; T-LYMPHOCYTES;

EID: 0022504844     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(86)80124-X     Document Type: Article

References (15)

1. Further delineation of the 10p deletion syndrome
2. Separation of leukocytes from blood and bone marrow
3. Biological effects of anti-immunoglobulins: evidence for immunoglobulin receptors on “T” and “B” lymphocytes
4. The human rosetteforming cells as a marker of a population of thymus-derived cells
5. Radioimmunoassay for the middle region of human parathyroid hormone using an homologous antiserum with carboxyterminal fragment of bovine parathyroid hormone as radioligand
6. Partial monosomy of chromosome 10 short arms
7. A child trisomic for the distal part of chromosome 14q
8. A deletion in chromosome 22 can cause DiGeorge syndrome
9. The association of the DiGeorge anomalad with partial monosomy of chromosome 22
10. Familial DiGeorge syndrome and associated partial monosomy of chromosome 22
11. The spectrum of DiGeorge syndrome
12. Clinical and immunologic spectrum of the DiGeorge syndrome
13. DiGeorge syndrome in monozygotic twins: treatment with calcitriol
14. Partial DiGeorge syndrome with substantial cell-mediated immunity