Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?

Joint Authors

Laccetta, Gianluigi
Toschi, Benedetta
Bertini, Veronica
Valetto, Angelo
Consolini, Rita
Fogli, Antonella

Source

Case Reports in Pediatrics

Issue

Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-3, 3 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2015-12-17

Country of Publication

Egypt

No. of Pages

3

Main Subjects

Medicine

Abstract EN

We report a case of DiGeorge-like syndrome in which immunodeficiency coexisting with juvenile idiopathic arthritis, congenital heart disease, delay in emergence of language and in motor milestones, feeding and growing problems, enamel hypoplasia, mild skeletal anomalies, and facial dysmorphisms are associated with no abnormalities found on genetic tests.

American Psychological Association (APA)

Laccetta, Gianluigi& Toschi, Benedetta& Fogli, Antonella& Bertini, Veronica& Valetto, Angelo& Consolini, Rita. 2015. Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?. Case Reports in Pediatrics،Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1059819

Modern Language Association (MLA)

Laccetta, Gianluigi…[et al.]. Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?. Case Reports in Pediatrics No. 2015 (2015), pp.1-3.
https://search.emarefa.net/detail/BIM-1059819

American Medical Association (AMA)

Laccetta, Gianluigi& Toschi, Benedetta& Fogli, Antonella& Bertini, Veronica& Valetto, Angelo& Consolini, Rita. Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?. Case Reports in Pediatrics. 2015. Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1059819

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1059819