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An association syndrome described only once in two sisters. They had a 46,XY karyotype, cleft lip and palate, preauricular pits and a \'squashed down\' appearance because of a short columella and small nares. Other anomalies included broad hands and feet, and a hypermuscular appearance. Cardiac, renal, musculoskeletal and ectodermal anomalies were also present. Ectodermal defects included \'punched out scalp defects\' and unusual positioning of hair whorls. They also had short stature, streak gonads, and mild developmental delay.
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