WordNet

a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
of or relating to immunology (同)immunologic

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Stagi S1, Gulino AV2, Lapi E3, Rigante D4.
Immunologic research.Immunol Res.2016 Apr;64(2):345-59. doi: 10.1007/s12026-015-8707-4.
Kabuki syndrome (KS) is a rare multi-systemic disorder characterized by a distinct face, postnatal growth deficiency, mild-to-moderate intellectual disability, skeletal and visceral (mainly cardiovascular, renal, and skeletal) malformations, dermatoglyphic abnormalities. Its cause is related to muta
PMID 26411453

Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS.

Saida S1, Umeda K1, Yasumi T1, Matsumoto A1, Kato I1, Hiramatsu H1, Ohara O2, Heike T1, Adachi S3.
Pediatric transplantation.Pediatr Transplant.2016 Mar;20(2):333-6. doi: 10.1111/petr.12667. Epub 2016 Jan 8.
A 13-yr-old boy bearing lymphedema and congenital deafness had distinct hematological abnormalities consisting of reduced monocytes, B cells, and dendritic cells in the peripheral blood as well as MDS with normal karyotype in the bone marrow. The patient was diagnosed with Emberger syndrome by seque
PMID 26748574

Congenital heart block related to maternal autoantibodies: descriptive analysis of a series of 18 cases from a single center.

Doti PI1, Escoda O1, Cesar-Díaz S2, Palasti S1, Teixidó I3, Sarquella-Brugada G2, Gómez O3, Martínez JM3, Espinosa G4.
Clinical rheumatology.Clin Rheumatol.2016 Feb;35(2):351-6. doi: 10.1007/s10067-016-3174-4. Epub 2016 Jan 20.
The objective of this study was to describe the clinical and immunological characteristics of maternal autoimmune-mediated fetal congenital heart block (CHB) in a cohort of pregnant women from an autoimmune disease pregnancy clinic. This is a retrospective observational study of all women presenting
PMID 26791874