Neonatal Death Suspected To Be From Sepsis Was Found To Be Kernicterus With G6PD Deficiency

被引:20
作者
Christensen, Robert D. [1 ]
Yaish, Hassan M. [2 ,5 ]
Wiedmeier, Susan E. [2 ,6 ]
Reading, N. Scott [7 ]
Pysher, Theodore J. [3 ,4 ]
Palmer, Cheryl Ann [3 ,4 ]
Prchal, Josef T. [3 ,4 ,7 ]
机构
[1] Intermt Healthcare, Women & Newborns Program, Salt Lake City, UT USA
[2] Univ Utah, Sch Med, Dept Pediat, Salt Lake City, UT USA
[3] Univ Utah, Sch Med, Dept Pathol, Salt Lake City, UT USA
[4] Univ Utah, Sch Med, Dept Internal Med, Div Hematol Oncol, Salt Lake City, UT USA
[5] ARUP Labs, Div Hematol Oncol, Salt Lake City, UT USA
[6] ARUP Labs, Div Neonatol, Salt Lake City, UT USA
[7] ARUP Labs, Special Genet Lab, Salt Lake City, UT USA
关键词
kernicterus; jaundice; neonate; hemolysis; G6PD; Mahidol mutation; GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY; POTENTIAL CAUSE; HYPERBILIRUBINEMIA; PHOTOTHERAPY; MUTATIONS; NEWBORNS;
D O I
10.1542/peds.2013-1030
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We cared for a term male infant born to Burmese immigrants. At about 24 hours a total serum bilirubin (TSB) was 9.3 mg/dL, and phototherapy was begun. It was stopped 48 hours later, with a TSB of 10.9 mg/dL, and he was discharged from the hospital with an appointment for a repeat TSB check 48 hours later. A few hours before the appointment he became listless and apneic, and his parents took him to the emergency department of the regional children's hospital, where sepsis was suspected. The TSB was 41 mg/dL. He died 4 hours later, despite intensive care efforts, with opisthotonus and refractory hypotension. Blood drawn before the exchange transfusion had low glucose-6-phosphate dehydrogenase (G6PD) enzymatic activity, and sequencing of the G6PD gene revealed the G6PD Mahidol mutation (c. 487G > A). Cultures and postmortem examination did not demonstrate an infectious process, but kernicterus was present. Acute kernicterus can mimic septic shock.
引用
收藏
页码:E1694 / E1698
页数:5
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