Pierre Robin syndrome
Pierre Robin sequence
Robin's anomalad

Pierre Robin syndrome is named after him.

The most severe problem associated with Stickler syndrome is Pierre Robin syndrome.

Shannon Pierce was distraught three years ago when she learned that her baby, Caroline, had Pierre Robin syndrome, a rare congenital disorder.

Pierre Robin syndrome refers to a sequence of abnormalities that may occur as a distinct syndrome or as part of another underlying disorder.

Examples of first arch syndromes include Treacher Collins syndrome and Pierre Robin syndrome.

Children with Pierre Robin syndrome are born with facial deformities like abnormally small lower jaws and cleft palates that can hinder eating and breathing.

Often these syndromes are not recognized in a family until a baby is born with Pierre Robin syndrome or some members have detached retinas or cataracts at a young age.

Catel-Manzke syndrome is a rare genetic disorder characterized by distinctive abnormalities of the index fingers; the classic features of Pierre Robin syndrome; occasionally with additional physical findings.

Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin sequence, Pierre Robin anomaly or Pierre Robin anomalad), is a congenital condition of facial abnormalities in humans.

A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome.

It is one of the features of Pierre Robin Sequence and Down Syndrome.

These syndromes include Treacher Collins syndrome and Pierre Robin sequence.

SATB2 was found to be disrupted in two unrelated cases with de novo apparently balanced chromosome translocations associated with cleft palate and Pierre Robin Sequence.

Persons with Pierre Robin sequence (PRS) are at greater risk for hearing impairment than persons with cleft lip and/or palate without PRS.

In the circumstance that misarticulation is caused by physiological abnormalities such as the Pierre Robin Sequence or banded lingual frenulum, treatment may rarely involve surgical intervention, but further therapeutic treatment is still necessary.

It has been concluded that individuals with Franceschetti syndrome or Pierre Robin sequence are at increased risk for developing airway obstruction following pharyngoplasty due to their shallow nasopharyngeal airway and inadequate maxillofacial growth at the time of the surgery.

Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin sequence, Pierre Robin anomaly or Pierre Robin anomalad), is a congenital condition of facial abnormalities in humans.