Fig. 2From: Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePhenotypes of proband IV1 and brother IV3. a, b Proband’s facial features with high forehead, prominent nose, and sparse eyebrows and eyelashes. c Scleral pigmentation in proband. d, e Facial features with high forehead, prominent nose sparse eyebrows and eyelashes, and unilateral ptosis in brother IV3. f Scleral pigmentation in brother IV3Back to article page