2013
DOI: 10.1007/s10875-013-9937-7
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Phenotypic Parameters Predict Time to Normalization in Infants with Hypogammaglobulinemia

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Cited by 9 publications
(4 citation statements)
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“…One of them, transient hypogammaglobulinaemia of infancy (THI), is a heterogeneous disorder characterised by reduced serum IgG (often IgA and sometimes also IgM) level in early childhood and recurrent infections, mostly of the respiratory tract [24-26]. A putative diagnosis is initially made after exclusion of other causes of hypogammaglobulinaemia, while a definitive diagnosis of THI can only be made retrospectively in patients with normalised IgG levels and withdrawal of clinical symptoms, which occurs usually between the second and fourth year of life [27]. The underlying definitive basis of this disorder is still unknown.…”
Section: Introductionmentioning
confidence: 99%
“…One of them, transient hypogammaglobulinaemia of infancy (THI), is a heterogeneous disorder characterised by reduced serum IgG (often IgA and sometimes also IgM) level in early childhood and recurrent infections, mostly of the respiratory tract [24-26]. A putative diagnosis is initially made after exclusion of other causes of hypogammaglobulinaemia, while a definitive diagnosis of THI can only be made retrospectively in patients with normalised IgG levels and withdrawal of clinical symptoms, which occurs usually between the second and fourth year of life [27]. The underlying definitive basis of this disorder is still unknown.…”
Section: Introductionmentioning
confidence: 99%
“…Tekrarlayan enfeksiyon öyküsü bulunan çocuklarda bağışıklığın kontrolü önem taşımaktadır. İmmünoglobulin replasman tedavisinin hangi durumlarda verilmesi gerektiği halen tartışmalıyken, IVIG tedavisinin immünoglobulin değerlerindeki düzelme süresini olumlu etkilediği de bilinmektedir (14). Çalışmamızda antikor eksikliği tanısı alan çocukların retrospektif olarak değerlendirilmiş olması, antikor eksikliğine bağlı immün yetmezlikler alt grup tanı ve tetkikleri merkezimizde analiz edilememiş olması çalışmamızın kısıtlı yanlarıdır.…”
Section: Bulgularunclassified
“…40 This is called selective IgA deficiency (IGAD). 68,71 High total B cells, low memory B cells and reduced CD19 on B cells have been described in patients with THI. As with CVID, due to rapid immune system development in children and wider normal ranges of immunoglobulin levels in early childhood, it is not appropriate to confer a diagnosis of IGAD below begins.…”
Section: Iga Deficiencymentioning
confidence: 99%
“…Transient hypogammaglobulinemia of infancy (THI) is an IgG deficiency that begins in infancy and resolves spontaneously by 5 years of age. 19,68,69,71 By definition, IgG is lower than normal for age.…”
Section: Iga Deficiencymentioning
confidence: 99%