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Synonyms of Pierre Robin Sequence

Glossoptosis, Micrognathia, and Cleft Palate
Pierre Robin
Pierre Robin Anomalad
Pierre Robin Complex
Pierre Robin Deformity
Pierre Robin Malformation Sequence
Pierre Robin Syndrome
Pierre Robin Triad
Robin Anomalad
Robin Complex
Robin Syndrome

General Discussion

Pierre Robin sequence is characterized by an unusually small lower jaw (micrognathia) and downward displacement
of the tongue (glossoptosis). Some infants also have an abnormal opening in the roof of the mouth (cleft palate);
both the soft and hard palate can be affected.

Signs & Symptoms

The downward placement of the tongue, coupled with an unusually small jaw, may obstruct normal breathing and
cause respiratory distress, feeding problems, and failure to thrive. Sleep disorders, including obstructive sleep
apnea, a condition in which breathing temporarily stops, may occur.

Cardiovascular and lung conditions, such as benign heart murmurs, high blood pressure in the arteries of the lungs
(pulmonary hypertension), and narrowing of the opening between the lung artery and the right ventricle of the heart
(pulmonary stenosis) are possible manifestations of the disease. Anomalies of the musculoskeletal system, including
those in the arms, legs, feet, and vertebral column, are also common. Inflammation of the middle ear (otitis media)
occurs in about 80% of patients. Eye (ocular) defects are noted in about 10% to 30% of patients.


At present, the exact cause of Pierre Robin sequence is unknown. The most widely held view is that failure of the
lower jaw to fully develop early in gestation causes the tongue to be positioned high in the oral cavity, which, in turn,
prevents palate closure. The disease can occur by itself, and less commonly, as a feature in multiple defect

Pierre Robin sequence appearing with no underlying disorder may be inherited as an autosomal recessive trait.
Genetic diseases are determined by the combination of genes for a particular trait that are on the chromosomes
received from the father and the mother.

Recessive genetic disorders occur when an individual inherits the same abnormal gene for the same trait from each
parent. If an individual receives one normal gene and one gene for the disease, he or she will be a carrier of the
disease, but usually will not show symptoms. The risk of two carrier parents both passing the defective gene and
having an affected child is 25% with each pregnancy. The risk of having a child who is a carrier like the parents is
50% with each pregnancy. The chance of having a child who receives normal genes from both parents and is
genetically normal for that particular trait is 25%. The risk is the same for males and females.

All individuals carry 4-5 abnormal genes. Parents who are close relatives (consanguineous) have a higher chance
than do unrelated parents of both carrying the same abnormal gene, which increases the risk of having children with
a recessive genetic disorder.

Affected Populations

Pierre Robin sequence affects males and females in equal numbers, with a prevalence of about one in 8,500 births.

Related Disorders

Disease comparisons may be useful for a differential diagnosis. Symptoms of Stickler syndrome, cerebro-costo-
mandibular syndrome, and Treacher Collins syndrome can be similar to those of Pierre Robin sequence.

Stickler syndrome is a rare genetic progressive connective tissue disorder that affects the eyes, ears, face, joints,
and bones. Signs and symptoms may include: nearsightedness (myopia), detached retina (separation of the retina of
the eye from the layers of the eyeball that support it), hearing loss, flat face with a small nose, and joint pain. It is also
characterized by two features of Pierre Robin sequence: unusually small lower jaw (micrognathia) and cleft palate.
(For more information on this disorder, choose Stickler as your search term in the Rare Disease Database.)

Cerebro-costo-mandibular syndrome is a rare genetic disorder characterized by the features of Pierre Robin
sequence, plus rib and chest cavity (thorax) defects. Other disease features may include feeding, breathing, and
speech difficulties. Occasionally, an unusually small head, mental retardation, abnormally placed fifth fingers, and
bone abnormalities also occur. (For more information on this disorder, choose Cerebro-Costo-Mandibular as your
search term in the Rare Disease Database.)

Treacher Collins syndrome is a rare genetic disorder characterized by deformities in the jaw and ears with deafness,
cleft palate, and unusually slanted eyes. Cheekbones may be very small or partially absent. (For more information
on this disorder, choose Treacher Collins as your search term in the Rare Disease Database.)

Other related syndromes and conditions include: trisomy aaq syndrome, trisomy 18 syndrome, velocardiofacial
(Shprintzen) syndrome, deletion 4q syndrome, rheumatoid arthropathy, hypochondroplasia, Mobius syndrome, and
CHARGE association.

Standard Therapies

Pierre Robin sequence can be detected while the fetus is still in the womb using ultrasound imaging.

Infants with Pierre Robin sequence should be observed closely for breathing difficulties. A tube may be inserted in
the infant's throat (intubation) or a surgical opening may be made into the trachea through the neck (tracheostomy)
to assist the infant in breathing.

Surgery to close the palate is typically performed between 12 and 18 months of age. Doctors may postpone the
corrective surgery, however, to allow the opening in the palate to close on its own as natural growth occurs. If
speech is impaired, a child with a cleft palate should participate in speech therapy or be monitored by a speech

A child with a cleft palate is susceptible to fluid build-up in the ears, which can affect hearing and also lead to ear
infections. Monitoring by an ear, nose and throat specialist and an audiologist is recommended for children with ear
and hearing problems.

Surgery to improve the appearance of the jaw is rarely necessary because the small lower jaw seen at birth most
often grows to a more normal size by 18 months of age.

Genetic counseling may be of benefit for patients and their families. Symptomatic and supportive treatment may also
be useful.

Investigational Therapies

Information on current clinical trials is posted on the Internet at All studies receiving U.S.
government funding, and some supported by private industry, are posted on this government Web site.

For information about clinical trails being conducted at the National Institutes of Health (NIH) Clinical Center in
Bethesda, MD, contact the NIH Patient Recruitment Office:

Tollfree: (800) 411-1222

TTY: (866) 411-1010


For information about clinical trials sponsored by private sources, contact:

NORD Member Organizations

Childrens Craniofacial Association
13140 Coit Road
Suite 517
Dallas, TX 75240 USA
Phone: (214) 570-9099
Toll-free: (800) 535-3643

Other Organizations
Birth Defect Research for Children, Inc.
976 Lake Baldwin Lane
Orlando, FL 32814 USA
Phone: (407) 895-0802

Cleft Lip and Palate Foundation of Smiles
2044 Michael Ave SW
Wyoming, MI 49509
Phone: (616) 329-1335

FACES: The National Craniofacial Association

PO Box 11082
Chattanooga, TN 37401
Phone: (423) 266-1632
Toll-free: (800) 332-2373

Genetic and Rare Diseases (GARD) Information Center

PO Box 8126
Gaithersburg, MD 20898-8126
Phone: (301) 251-4925
Toll-free: (888) 205-2311

Let Them Hear Foundation

1900 University Avenue, Suite 101
East Palo Alto, CA 94303
Phone: (650) 462-3174

Pierre Robin Network

3604 Biscayne
Quincy, IL 62305 USA
Phone: (217) 224-0698

Pierre Robin Sequence

Pierre Robin Sequence



Wilcox BK, Tatum SA. Cerebro-costo-mandibular syndrome presenting as Pierre Robin sequence. Am J Otolaryngol.
2004 Jul-Aug;25(4)258-62.

Yao CT, Wang JN, Tai YT, Tsai TY, Wu JM. Successful management of a neonate with Pierre-Robin syndrome and
severe upper airway obstruction by long-term placement of a laryngeal mask airway. Resuscitation. 2004

Poos A. Pierre Robin Sequence. Wide Smiles Web site. Available at:
901.html. Accessed November 11, 2004.
Tewfik TL, Trinbh N, Teebi AS. Pierre Robin Syndrome. Emedicine Web site. Available at
Accessed November 11, 2004.


Sticklers syndrome. Available at Mayo Clinic Web site:

Accessed November 15, 2004.

Treacher Collins syndrome. Childrens Craniofacial Association Web site. Available at: Accessed November 15, 2004.

Online Mendelian Inheritance in Man (OMIM). Victor A. McKusick, editor; Johns Hopkins University, Last Edit Date
9/19/1002. Entry Number 261800.

Years Published
1989, 1996, 2004

The information in NORDs Rare Disease Database is for educational purposes only and is not intended to replace the advice
of a physician or other qualified medical professional.

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