Corpus Callosum Agenesia and Lymfopenia. Case Report 2 e child of non-related parents Healthy sister No familial history.

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Corpus Callosum Agenesia and Lymfopenia

Case Report 2 e child of non-related parents Healthy sister No familial history

Born at 38 weeks GG 3485 gr First week of life event free After first week failure to thrive recurrent episodes of fever

Physical examination Hypotonia, opistotonus G 3960 gram Kinky hair Cataract right eye High palatum Enlarged liver and spleen

Westeinde op 13/6 (lft. 7 weken) voor failure to thrive Urineweginfectie 15/6 LP: bloederig: vermoeden intra-cerebrale bloeding: verwijzing JKZ

Neurologisch MRI brain: corpus callosum agenesia Opistotonos Hypotonie Microcefalia High palatum Elevated CK EyesCataract VEP: blindness of cerebral origin

Hematological findings Several episodes of Normocytaire anemia with reticulocytosis Coombs negatif Bilirubine normal No signs of occult blood loss

Gastro enterological findings Elevated Liver enzymes AST 255 U/L ALT 139 U/L LDH 1240 U/L Ferritin max mg/l

Immunological findings Recurrent fever (3 days/week) Persistent and chronic Candida Albicans infection Very few positive cultures 1x pos. E. Vulneri Urine Proteus Urine Klebsiella

Cardial complication Severe Myocarditis with admission for several weeks. Recovered No infectious agent shown

leucocyts lymphocyts CD CD3+CD CD3+CD CD3- CD56+CD16+/ CD3-CD56+CD CD CD CD4 RA CD4 RO CD8 RA CD8 RO CD19 CD272%5%4%

T cell stimulation tests PHA: 400 (> 17000) CD2-CD28: (>17000) CD3: 70 (> 1500) CD3-CD28: 7000 (> 17000) Background 105 (< 500)

Immuunglobulines 1 month8 months IgA 0.4 g/l0.44 g/l IgM 0.3 g/l0.67 g/l IgG 4.5 g/l4.59 g/l IgD Normal Normal respons to vaccination

Diagnosis? Mitochondrial depletion Syndrome? Fatal neonatal-onset mitochondrial respiratory chain disease with T cell immunodeficiency. Reichenbach et al Pediatr Res Sep;60(3):321-6.

Severe recurrent infectious diseases Anemia, and thrombocytopenia. Severe psychomotor retardation, Axial hypotonia, Disturbed pain perception Hypoplasia of corpus callosum Impaired myelinization of the temporo- occipital region

Lack of CD8(+) T lymphocytes and NK cells Decrease CD45RO- CD8(+) lymphocytes Diminished Activation of T lymphocytes via IL-2

Conclusion Infant with recurrent fever, chronic Candida Albicans infection and multiple neurological problems T-cel penia (CD8, CD4 to a lesser extent) Bad proliferation respons to CD3, PHA Probably normal B cell compartment Normal NK cells Mitochondrial DNA depletion syndrome?