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Fig. 2 | Human Genomics

Fig. 2

From: Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree

Fig. 2

Phenotypes 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 IV3

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