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Feingold syndrome type 2

rare

Feingold syndrome type 2 (FS2) is a rare inherited malformation syndrome characterized by skeletal abnormalities and mild intellectual disabilities similar to those seen in Feingold syndrome type 1 (FS1) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures.

Causal genes
MIR17HG
Also known as
brachydactyly-short stature-microcephaly syndrome · Brunner-Winter syndrome type 2 · Feingold syndrome 2 · FGLDS2 · FS2

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