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. Author manuscript; available in PMC: 2010 Dec 23.
Published in final edited form as: Ophthalmic Genet. 2010 Mar;31(1):24–29. doi: 10.3109/13816810903426249

TABLE 1.

Patient’s medical history and clinical features consistent with del22q11.2 syndrome

Asthma Hypoplastic thymus gland
Eczema Neonatal hypocalcemia
Seasonal allergy Right-sided aortic arch, bicuspid aortic valve
Recurrent pneumonia (childhood) Partial cleft palate
Recurrent cold sores (childhood) Focal deformity & hypoplasia of the 1st and 2nd ribs
Recurrent otitis media Mild neurosensory hearing loss
Tonsillectomy Atypical facies
Measles, chickenpox (childhood)
Chronic sinusitis
Migraine