Page last updated: 2024-10-16

ammonium hydroxide and DiGeorge Syndrome

ammonium hydroxide has been researched along with DiGeorge Syndrome in 1 studies

azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.

DiGeorge Syndrome: Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies.

Research Excerpts

ExcerptRelevanceReference
"Several genetic chromosomal abnormalities, including 22qDS, and CPSS have similar symptoms, and neurodevelopmental abnormalities, particularly those caused by PSE, may be difficult to diagnose."1.72Congenital portosystemic venous shunt associated with 22q11.2 deletion syndrome: a case report. ( Ifuku, T; Nagatomo, Y; Nakatani, K; Suzuki, S; Yamamura, Y; Yokoyama, R, 2022)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Ifuku, T1
Suzuki, S1
Nagatomo, Y1
Yokoyama, R1
Yamamura, Y1
Nakatani, K1

Other Studies

1 other study available for ammonium hydroxide and DiGeorge Syndrome

ArticleYear
Congenital portosystemic venous shunt associated with 22q11.2 deletion syndrome: a case report.
    BMC pediatrics, 2022, 06-29, Volume: 22, Issue:1

    Topics: Ammonia; Bile Acids and Salts; Child, Preschool; Chromosome Aberrations; DiGeorge Syndrome; Humans;

2022