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Chromosome 14;16 translocation
Blepharophimosis
A fixed reduction in the vertical distance between the upper and lower eyelids with short palpebral fissures. [from HPO]
Uniparental disomy of maternal origin
Motor developmental delay due to 14q32.2 paternally expressed gene defect
Temple syndrome is a short stature disorder of imprinting. The cardinal features are low birth weight, hypotonia and motor delay, feeding problems early in life, early puberty, and significantly reduced final height. Facial features include a broad forehead and short nose with a wide nasal tip, and the majority of patients have small hands and feet. However, many of the clinical features are nonspecific, making diagnosis difficult. In addition, isodisomy may uncover recessive disorders, which may influence the phenotype in maternal uniparental disomy of chromosome 14 (UPD14mat) cases (summary by Ioannides et al., 2014). [from OMIM]
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