Williams syndrome

Williams syndrome (WS) is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, underdeveloped chin, short nose and full cheeks. [Source: Wikipedia ]

Synonyms
Idiopathic hypercalcemia
Williams-Beuren syndrome
OrphaNet reference
Williams syndrome 
May Cause
Absent nose
Altered calcium concentration
Altered phosphorus concentration
Anodontia or hypodontia
Aortic insufficiency
Aortic valve disease
Arterial calcification
Arterial occlusion
Bladder diverticulum
Bladder wall calcification
Camptodactyly
Clinodactyly
Clinodactyly of fifth finger
Congenital generalized osteoporosis
Congenital heart disease
Congenital premature craniosynostosis
Congenital prognathism
Congenital vertebral abnormality
Congenital widespread osteosclerosis
Craniosynostosis
Defective dentition
Delayed dentition
Delayed tooth eruption
Dense epiphyses of hands and feet
Dense or thick skull
Dense subchondral zone of vertebra
Densely sclerotic vertebra
Dental defect
Depressed nasal bridge
Diffusely dense skull base
Eyebrow anomaly
Hypercalcemia
Hypercalciuria
Hyperechoic renal cortex
Hyperechoic renal medulla
Hypotelorism
Intracranial calcification
Kyphoscoliosis
Left ventricular enlargement
Medially flared eyebrows
Medullary nephrocalcinosis
Microdontia
Micrognathia
Multiple intracranial calcification
Nail aplasia
Nail deformity
Nail dystrophy
Nail hypoplasia
Osteosclerosis
Precocious puberty
Pulmonary artery branch stenosis
Pulmonary artery stenosis
Pulmonary hypertension
Radiolucent metaphyseal bands
Radioulnar synostosis
Renal cystic disease
Rickets
Small aortic arch
Small ascending aorta
Small nose
Soft-tissue calcification
Strabismus
Supravalvular aortic stenosis
Systemic hypertension
Thick skull
Transverse dense metaphyseal bands
Urinary tract calculus
Vascular calcification
Wide metaphysis
Widespread osteosclerosis
Widespread osteosclerosis of medullary and cortical bone
Widespread soft-tissue calcification
Idiopathic hypercalcemia
Williams-Beuren syndrome
Absent nose
Altered calcium concentration
Altered phosphorus concentration
Anodontia or hypodontia
Aortic insufficiency
Aortic valve disease
Arterial calcification
Arterial occlusion
Bladder diverticulum
Bladder wall calcification
Camptodactyly
Clinodactyly
Clinodactyly of fifth finger
Congenital generalized osteoporosis
Congenital heart disease
Congenital premature craniosynostosis
Congenital prognathism
Congenital vertebral abnormality
Congenital widespread osteosclerosis
Craniosynostosis
Defective dentition
Delayed dentition
Delayed tooth eruption
Dense epiphyses of hands and feet
Dense or thick skull
Dense subchondral zone of vertebra
Densely sclerotic vertebra
Dental defect
Depressed nasal bridge
Diffusely dense skull base
Eyebrow anomaly
Hypercalcemia
Hypercalciuria
Hyperechoic renal cortex
Hyperechoic renal medulla
Hypotelorism
Intracranial calcification
Kyphoscoliosis
Left ventricular enlargement
Medially flared eyebrows
Medullary nephrocalcinosis
Microdontia
Micrognathia
Multiple intracranial calcification
Nail aplasia
Nail deformity
Nail dystrophy
Nail hypoplasia
Osteosclerosis
Precocious puberty
Pulmonary artery branch stenosis
Pulmonary artery stenosis
Pulmonary hypertension
Radiolucent metaphyseal bands
Radioulnar synostosis
Renal cystic disease
Rickets
Small aortic arch
Small ascending aorta
Small nose
Soft-tissue calcification
Strabismus
Supravalvular aortic stenosis
Systemic hypertension
Thick skull
Transverse dense metaphyseal bands
Urinary tract calculus
Vascular calcification
Wide metaphysis
Widespread osteosclerosis
Widespread osteosclerosis of medullary and cortical bone
Widespread soft-tissue calcification