ConditionsEnlarged fontanelDelayed closure
Most common
Achondroplasia
Congenital hypothyroidism
Down syndrome
Increased intracranial pressure
Normal variation
Familial macrocephaly
Rickets
Less common
Skeletal disorders
Acrocallosal syndrome (seizures, polydactyly, mental retardation)
Apert's syndrome (craniosynostosis, proptosis, hypertension)
Campomelic dysplasia (prenatal growth deficiency, large cranium, bowed legs)
Hypophosphatasia (polyhydramnios, short, deformed limbs, soft skull)
Kenny-Caffey syndrome (hypoparathyroidism, dwarfism, macrocephaly)
Osteogenesis imperfecta (shortened limbs, wormian calvarial bones)
Chromosomal abnormalities
Trisomy 13 (polydactyly, microcephaly, cleft lip and palate)
Trisomy 18 (growth retardation, small cranium, open metopic suture)
Congenital infections
Rubella (low birth weight, cataracts, “blueberry muffin” skin lesions)
Syphilis (saddle nose deformity, joint swelling, maculopapular rash)
Drugs and toxins
Aminopterin-induced malformation (craniosynostosis, absences of frontal bones, hypertelorism)
Fetal hydantoin syndrome (microcephaly, broad nasal bridge, hypoplasia of nails)
Dysmorphogenetic syndromes
Beckwith-Wiedemann syndrome (macrosomia, abdominal wall defect, macroglossia)
Zellweger syndrome (high forehead, flat occiput, abnormal ears, hypotonia)
Cutis laxa (pendulous skin folds, hoarse cry)
VATER association (vertebral defects, anal atresia, tracheoesophageal fistula, renal dysplasia)
Otopalatodigital syndrome (frontal bossing, broad terminal phalanges, syndactyly)
Miscellaneous
Malnutrition (poor weight gain, asymmetric growth)
Hydranencephaly (macrocephaly, thinned skull vault, primitive reflexes preserved)
Intrauterine growth retardation (birth weight less than 2 standard deviations below mean)