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Fig. 1 | Pediatric Rheumatology

Fig. 1

From: A20 haploinsufficiency in a neonate caused by a large deletion on chromosome 6q

Fig. 1

Clinical manifestations and genetic characteristics. A Daily maximum core temperature in the neonate from Day 23 post-birth. B Hemoglobin (g/L) levels measured during febrile episodes, as well as basal levels measured at birth and follow-up (green arrows denote infusions of hemoglobin). C Circulating concentrations of alanine transaminase (ALT; IU/L, blue quadrangle) and aspartate transaminase (AST; IU/L, purple triangle) over time. D Fluctuation of blood serum CMV-DNA levels (103 copies/mL); the black arrow indicates initiation of ganciclovir treatment. E A large deletion in chromosome 6 and OMIM genes encompassing the 6q23.2q24.3 region

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