[Clinical features and molecular diagnosis of three patients with DiGeorge anomaly].

Abstract

OBJECTIVE:

To investigate the clinical features and molecular diagnostic methods of three patients with DiGeorge anomaly.

METHOD:

The clinical manifestations and immunological features of the three cases with DiGeorge anomaly were analyzed. We detected the chromosome 22q11.2 gene deletion by fluorescence in situ hybridization (FISH).

RESULT:

(1) CLINICAL MANIFESTATIONS: All three cases had varying degrees of infection, congenital heart disease and small thymus by imaging; two cases had significant hypocalcemia (1.11 mmol/L and 1.22 mmol/L, respectively), accompanied by convulsions; only 1 case had cleft palate and all had no significant facial deformity. (2) Immunological characteristics: All three cases had varying degrees of T-cell immune function defects (percentage of T lymphocytes was 24% - 43%, absolute count was 309 - 803/µl), and levels of immunoglobulin G, A, M, and percent of B lymphocytes and absolute count were normal. (3) Detection of the chromosome 22q11.2 gene deletion: 400 cells of each case were detected. All cells showed two green and one red hybridization signal, indicating the presence of gene deletions in chromosome 22q11.2. (4) OUTCOME: All three cases were treated with thymosin, and appropriate clinical intervention for cardiac malformations, hypocalcemia, and were followed-up for 4 - 18 months, the prognosis was good.

CONCLUSION:

DiGeorge anomaly showed diverse clinical manifestations. We should consider the disease if patients had congenital heart disease, thymic hypoplasia, hypocalcemia and/or impaired immune function. FISH for detecting chromosome 22q11.2 gene deletion can be used as accurate and rapid diagnostic method. Thymosin treatment and other clinical intervention may help to improve the prognosis of patients with partial DiGeorge anomaly.

• Authors: Jin-qiao Sun, Lai-shuan Wang, Chun-hua Qi, Wen-jing Ying, Xiao-hong Guo, Dan-ru Liu, Xiao-ying Hui, Fang Liu, Yun Cao, Fei-hong Luo, Xiao-chuan Wang
• Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics (Zhonghua Er Ke Za Zhi) Vol. 50 Issue 12 Pg. 944-7 (Dec 2012) ISSN: 0578-1310 [Print] China
• PMID: 23324155 (Publication Type: Case Reports, English Abstract, Journal Article, Research Support, Non-U.S. Gov't)

Topics

• Cells, Cultured
• Chromosome Deletion
• Chromosomes, Human, Pair 22 (genetics)
• DiGeorge Syndrome (diagnosis, genetics, immunology)
• Female
• Heart Defects, Congenital (diagnosis, genetics)
• Humans
• Hypocalcemia (diagnosis, genetics)
• In Situ Hybridization, Fluorescence
• Infant, Newborn
• Male
• T-Lymphocytes (immunology)
• Thymus Gland (immunology, pathology)