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Blepharophimosis: The abnormal narrowness of the palpebral fissure in the horizontal direction caused by the lateral displacement of the medial canthi of the eyelids. (Dorland, 27th ed)Blepharoptosis: Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle.Eyelids: Each of the upper and lower folds of SKIN which cover the EYE when closed.Skin Abnormalities: Congenital structural abnormalities of the skin.Microstomia: A congenital defect in which the mouth is unusually small. (Dorland, 27th ed)Syndrome: A characteristic symptom complex.Abnormalities, MultipleChromosomes, Human, Pair 3: A specific pair of human chromosomes in group A (CHROMOSOMES, HUMAN, 1-3) of the human chromosome classification.Intellectual Disability: Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28)Forkhead Transcription Factors: A subclass of winged helix DNA-binding proteins that share homology with their founding member fork head protein, Drosophila.Pedigree: The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition.