BlepharophimosisBlepharoptosisSkin AbnormalitiesEyelidsRNA FoldingForkhead Transcription FactorsSyndromePrimary Ovarian InsufficiencyMutation, MissensePedigreeChromosomes, Human, Pair 3Genes, DominantNarrow Band ImagingFrameshift MutationAbnormalities, MultipleMutationMolecular Sequence DataChinaDNA Mutational AnalysisPhenotypeGenetic LinkageBase SequenceProtein TransportTranscription FactorsGene DeletionGenotypeDNA-Binding ProteinsAmino Acid SubstitutionSeverity of Illness Index