Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum
Author(s) -
Tomoko Fuke,
Akie Nakamura,
Takanobu Inoue,
Sayaka Kawashima,
Kaori Hara,
Keiko Matsubara,
Shinichiro Sano,
Kazuki Yamazawa,
Maki Fukami,
Tsutomu Ogata,
Masayo Kagami
Publication year - 2020
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/clinem/dgaa856
Subject(s) - microcephaly , genomic imprinting , macrocephaly , small for gestational age , uniparental disomy , short stature , genetics , medicine , pediatrics , biology , bioinformatics , dna methylation , chromosome , gestational age , gene , karyotype , pregnancy , gene expression
(Epi)genetic disorders associated with small-for-gestational-age with short stature (SGA-SS) include imprinting disorders (IDs). Silver-Russell syndrome (SRS) is a representative ID in SGA-SS and has heterogenous (epi)genetic causes.
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