Cornelia de Lange syndrome in Infant/Neonate
Growth retardation begins prenatally and is present throughout life. Mental development is also delayed in the majority of individuals, and some but not all have intellectual disabilities. The average intelligence quotient (IQ) is about 53. Seizures occur in about 1 in 4 individuals. Many patients are shy, with few social skills; patients sometimes have behavioral features of autism spectrum disorders. Middle ear infections are frequent and may result in a conductive hearing loss, while other patients have neurosensory hearing loss.
Limb and digital anomalies are common and may be asymmetric. These anomalies most commonly involve the upper limbs, which may be absent or severely reduced. Radioulnar fusion is an important sign. Digits are sometimes missing, but metacarpophalangeal malformations are more common. A shortened first metacarpal results in a proximally positioned thumb. A hypoplastic middle phalanx of the index finger is characteristic but not always present.
Cryptorchidism and hypoplastic genitalia are often present. Urinary infections have been reported in over 40% of patients. Cardiac septal defects and some degree of gastrointestinal dysfunction such as gastric reflux are common.
Q87.19 – Other congenital malformation syndromes predominantly associated with short stature
40354009 – De Lange syndrome
Differential Diagnosis & Pitfalls
Certain chromosomal aberrations such as duplication of bands 26-27 of the long arms of chromosome 3 and partial deletions of chromosome 2 can also mimic Cornelia de Lange syndrome. High-resolution karyotyping can be helpful in such cases.