Mitochondrial Disease as a Cause of Neonatal Hemophagocytic Lymphohistiocytosis

Table 1

Laboratory findings on admission.

CBC	WBC	25.3 × 10^3/μL
	Band	10%
	Seg	28.5%
	Lymph	47%
	Mono	11%
	Eosino	1.0%
	Baso	0%
	Blast	0%
	RBC	2.34 × 10^6/μL
	Hb	8.3 g/dL
	Ht	25.1%
	Plt	1.7 × /μL
	Ret	54.1
Coagulation	PT	37.1 sec
	APTT	110.7 sec
	Fib	40 mg/dL
	HPT	22.6%
	FDP	25.1  g/dL
	AT3	8.8%
Biochemistry findings	T-Bil	7.7 mg/dL
	D-Bil	0.2 mg/dL
	AST	47 IU/L
	ALT	6 IU/L
	CK	69 IU/L
	BUN	7 mg/dL
	Cr	0.61 mg/dL
	Na	138 mmol/L
	K	4.2 mmol/L
	Cl	109 mmol/L
	Ca	9.3 mg/dL
	P	5.7 mg/dL
	TP	3.2 g/dL
	ALB	2.0 g/dL
	NH3	156  g/dL
	Ferritin	3701.9 ng/mL
	CRP	1.23 mg/dL
Blood type	O Rh(+)
Immunological	IgG	333 mg/dL
	IgA	0 mg/dL
	IgM	12 mg/dL
	Direct Coombs test	(—)
Peripheral smear	Spherocytosis	(—)
	Elliptocytosis	(—)
Blood gas analysis (artery intubated)	pH	7.340
	O2	154.3 mmHg
	CO2	24.5 mmHg
		12.9 mmol/L
	BE	−10.8 mmol/L
	Lac	70.1 mg/dL
	Anion gap	16.1
Chromosomal test (G band)	46,XX

This table shows all laboratory findings on admission.
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