Multiple Bouts of Hypothermia and Shock in a Child with Gata-2 Mutation

We are reporting a 14-year-old male who presented at 12 years of age with recurrent episodes of hypothermia and bradycardia (30s) secondary to culture-negative septic shock from presumed viral respiratory illnesses. His temperatures on presentation are frequently below the level of detection rectally, with the lowest recorded temperature of 95.2F. Infectious testing during these episodes has only ever been positive for common respiratory viruses, including rhino/enterovirus and SARS-CoV-2. His episodes of hypothermia and shock have responded to supportive care, including warming and vasopressors. He has had 7 admissions in the past two years, with a duration of stay ranging from 4 to 23 days. There has been no decrease in length or frequency of admissions. He has also been found to have intermittent interstitial nodular lung disease on chest x-ray. A recent chest CT is normal. He has a kidney injury that has evolved into a nephrotic syndrome. No lymphedema. He has had persistent lymphopenia with intermittent pancytopenia. His lymphocyte subset numbers are low with an absolute CD4 count of 105 cells/μL, CD3A of 422 cells/μL, and absolute natural killer (NK) cells of 64 cells/μL. GM-CSF plasma <15.0 pg/mL during an acute episode. A bone marrow biopsy was performed, which only revealed hypocellularity. Concomitant problems include fetal alcohol syndrome and developmental delay. He has an intronic GATA2 c.1017+572C>T heterozygous mutation. He is on prophylaxis with atovaquone, voriconazole, and azithromycin and has received HPV vaccination. He was assessed for a stem cell transplant but was not considered a candidate. Discussion This patient’s GATA2 mutation is a single-nucleotide substitution located within intron 5 within the +9.5-enhancer element. Quantitatively, this may result in 50% reduction in GATA2 transcript levels. Not much is known about this mutation in these patients. His phenotype is different from other mutations in this gene because of recurrent hypothermia and shock. These episodes seem mostly linked with respiratory viral infections. There has been no reduction in frequency of these episodes, and now he is on homebound education.

Authors

Institutions

Publication Details

Journal
Journal of Human Immunity
Published
2026-05-01
DOI
https://doi.org/10.70962/cis2026abstract.78
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Multiple Bouts of Hypothermia and Shock in a Child with Gata-2 Mutation

Javeed Akhter, Kristin Hanscom, Zoya Khan, Michael Tekippe
Journal of Human Immunity
Congenital heart defects research
article

Multiple Bouts of Hypothermia and Shock in a Child with Gata-2 Mutation

Javeed Akhter, Kristin Hanscom, Zoya Khan, Michael Tekippe
article en

Abstract

We are reporting a 14-year-old male who presented at 12 years of age with recurrent episodes of hypothermia and bradycardia (30s) secondary to culture-negative septic shock from presumed viral respiratory illnesses. His temperatures on presentation are frequently below the level of detection rectally, with the lowest recorded temperature of 95.2F. Infectious testing during these episodes has only ever been positive for common respiratory viruses, including rhino/enterovirus and SARS-CoV-2. His episodes of hypothermia and shock have responded to supportive care, including warming and vasopressors. He has had 7 admissions in the past two years, with a duration of stay ranging from 4 to 23 days. There has been no decrease in length or frequency of admissions. He has also been found to have intermittent interstitial nodular lung disease on chest x-ray. A recent chest CT is normal. He has a kidney injury that has evolved into a nephrotic syndrome. No lymphedema. He has had persistent lymphopenia with intermittent pancytopenia. His lymphocyte subset numbers are low with an absolute CD4 count of 105 cells/μL, CD3A of 422 cells/μL, and absolute natural killer (NK) cells of 64 cells/μL. GM-CSF plasma <15.0 pg/mL during an acute episode. A bone marrow biopsy was performed, which only revealed hypocellularity. Concomitant problems include fetal alcohol syndrome and developmental delay. He has an intronic GATA2 c.1017+572C>T heterozygous mutation. He is on prophylaxis with atovaquone, voriconazole, and azithromycin and has received HPV vaccination. He was assessed for a stem cell transplant but was not considered a candidate. Discussion This patient’s GATA2 mutation is a single-nucleotide substitution located within intron 5 within the +9.5-enhancer element. Quantitatively, this may result in 50% reduction in GATA2 transcript levels. Not much is known about this mutation in these patients. His phenotype is different from other mutations in this gene because of recurrent hypothermia and shock. These episodes seem mostly linked with respiratory viral infections. There has been no reduction in frequency of these episodes, and now he is on homebound education.

Journal of Human ImmunityVol. 2(CIS2026)
Advocate Children's Hospital (US)
Quality Education
Openalex Percentile: Top 11%
Congenital heart defects research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.