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Hyper-IgM syndrome with CHARGE association.

Pilar Bahillo·Teresa Cantero·Pilar Solís·Paz Aragón·Samuel Gómez·Rosario Cambronero
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Abstract

A girl with coloboma of the iris, sensorineural deafness, growth delay, distinctive face, and cranial nerve dysfunction was diagnosed of CHARGE association in the first year of life. She presented with repeated otitis. At 3 yr of age, the patient suffered a septicemia (Streptococcus pneumoniae, Corynebacterium sp.). The immunoglobulin G (IgG) and IgA serum levels were decreased, IgM increased and cellular immunity parameters were normal, supporting the diagnosis of hyper-IgM (HIM) syndrome. The sequence of CD40 ligand and cytidine deaminase genes were normal. From then on, she was receiving immunoglobulin intravenously with an excellent outcome. Here, we report the first case of CHARGE association and HIM syndrome in the same patient. Although the cause could not be identified, a non-random link is likely.

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Abnormalities, MultipleChild, PreschoolChoanal AtresiaColobomaCranial Nerve DiseasesFaceFemaleGenitalia, FemaleGrowth DisordersHearing Loss, SensorineuralHeart Defects, CongenitalHumansHypergammaglobulinemiaImmunoglobulin AImmunoglobulin GImmunoglobulin MIrisOtitisSyndromeCase ReportsJournal Article

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Pilar Bahillo, Teresa Cantero, Pilar Solís, Paz Aragón, Samuel Gómez, Rosario Cambronero. 2003. Hyper-IgM syndrome with CHARGE association.. https://doi.org/10.1046/j.0905-6157.2003.00104.x

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