Noonan syndrome

Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. Facial features include widely spaced eyes, light-colored eyes, low-set ears, a short neck, and a small lower jaw. [Source: Wikipedia ]

OrphaNet reference
Noonan syndrome 
May Cause
Abnormal eyelashes
Abnormal sternum
Acyanotic congenital heart disease with normal pulmonary vascularity
Arterial dissection
Atrial septal defect
Body asymmetry
Brachydactyly
Broad middle phalanges
Camptodactyly
Cardiomyopathy
Cherubic facies
Chylothorax
Clinodactyly
Clinodactyly of fifth finger
Clubfoot
Coloboma
Congenital cardiomyopathy
Congenital elbow anomaly
Congenital foot deformity
Congenital fused vertebrae
Congenital heart disease
Congenital joint subluxation
Congenital macrocephaly
Congenital renal cystic disease
Congenital renal or ureteral anomaly
Congenital short hands and feet
Congenital skull defect
Congenital vertebral abnormality
Constrictive pericarditis
Cryptorchidism
Deafness
Delayed bone age
Depressed nasal bridge
Elbow dislocation
Exophthalmos
External ear malformation
Eyelid ptosis
Genital anomaly
Genu valgum
Hemangioma
Hydrops fetalis
Hypertelorism
Increased nuchal fold
Intestinal lymphangiectasia
Joint subluxation
Klippel-Feil syndrome
Kyphosis
Low hairline
Low-set ears
Lymphangiectasia
Macrocephaly
Madelung deformity
Metatarsus adductus
Microcephaly
Micrognathia
Multiple well-defined radiolucent jaw lesions
Myopia
Nail aplasia
Nail deformity
Nail dystrophy
Nail hypoplasia
Nipple anomaly
Nuchal cystic hygroma
Nystagmus
Odontogenic keratocyst
Pectus carinatum
Pectus excavatum
Pterygium
Pulmonary artery stenosis
Pulmonic stenosis
Retarded skeletal maturation
Rib anomaly
Scoliosis
Short foot
Short hand
Short narrow thoracic cage
Skin pigment abnormality
Strabismus
Thoracic dysplasia
Undersegmentation of sternum
Ventricular septal defect
Vertebral malsegmentation
Abnormal eyelashes
Abnormal sternum
Acyanotic congenital heart disease with normal pulmonary vascularity
Arterial dissection
Atrial septal defect
Body asymmetry
Brachydactyly
Broad middle phalanges
Camptodactyly
Cardiomyopathy
Cherubic facies
Chylothorax
Clinodactyly
Clinodactyly of fifth finger
Clubfoot
Coloboma
Congenital cardiomyopathy
Congenital elbow anomaly
Congenital foot deformity
Congenital fused vertebrae
Congenital heart disease
Congenital joint subluxation
Congenital macrocephaly
Congenital renal cystic disease
Congenital renal or ureteral anomaly
Congenital short hands and feet
Congenital skull defect
Congenital vertebral abnormality
Constrictive pericarditis
Cryptorchidism
Deafness
Delayed bone age
Depressed nasal bridge
Elbow dislocation
Exophthalmos
External ear malformation
Eyelid ptosis
Genital anomaly
Genu valgum
Hemangioma
Hydrops fetalis
Hypertelorism
Increased nuchal fold
Intestinal lymphangiectasia
Joint subluxation
Klippel-Feil syndrome
Kyphosis
Low hairline
Low-set ears
Lymphangiectasia
Macrocephaly
Madelung deformity
Metatarsus adductus
Microcephaly
Micrognathia
Multiple well-defined radiolucent jaw lesions
Myopia
Nail aplasia
Nail deformity
Nail dystrophy
Nail hypoplasia
Nipple anomaly
Nuchal cystic hygroma
Nystagmus
Odontogenic keratocyst
Pectus carinatum
Pectus excavatum
Pterygium
Pulmonary artery stenosis
Pulmonic stenosis
Retarded skeletal maturation
Rib anomaly
Scoliosis
Short foot
Short hand
Short narrow thoracic cage
Skin pigment abnormality
Strabismus
Thoracic dysplasia
Undersegmentation of sternum
Ventricular septal defect
Vertebral malsegmentation