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Annales de chirurgie plastique, 1996
This is a rare condition, but one which can cause severe problems in infancy. It can exist on its own, or as part of a wider group of rare syndromes all of which have the Pierre—Robin anomaly in addition to other features. Classification of these other syndromes is unclear at present.
A, LAMBERT, J, PSAUME
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This is a rare condition, but one which can cause severe problems in infancy. It can exist on its own, or as part of a wider group of rare syndromes all of which have the Pierre—Robin anomaly in addition to other features. Classification of these other syndromes is unclear at present.
A, LAMBERT, J, PSAUME
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The Indian Journal of Pediatrics, 1967
A typical case of the Pierre Robin syndrome is presented, and its management, both conservative and surgical, is discussed. Ouu case was mild and was successfully managed by the orthostatic technique of posturing and feeding.
A, Bhogaonker, K B, Sagor, O N, Bhakoo
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A typical case of the Pierre Robin syndrome is presented, and its management, both conservative and surgical, is discussed. Ouu case was mild and was successfully managed by the orthostatic technique of posturing and feeding.
A, Bhogaonker, K B, Sagor, O N, Bhakoo
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The hand in the Pierre Robin syndrome
The Journal of Hand Surgery, 1983In reviewing eight cases of children with the Pierre Robin syndrome, we found three cases to have abnormalities of the extremities such as syndactyly, hypoplastic digits, and a Poland syndrome. These hand abnormalities have not been previously emphasized in patients with the Pierre Robin syndrome.
V E, Wood, C, Sandlin
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Pierre Robin Syndrome in Siblings
Archives of Pediatrics & Adolescent Medicine, 1970Two cases of Pierre Robin syndrome in a sibship are reported. Two members of this family are carriers of a chromosome anomaly which appears to be unrelated to the syndrome.
R P, Singh, N T, Jaco, V, Vigna
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Sleep in Pierre Robin Syndrome
Chest, 1986Eight patients (aged 8 to 22 years) with the Pierre Robin syndrome underwent sleep studies. Seven demonstrated significant although minor degrees of increased sleep disturbances and apneas, and less time spent in the rapid-eye-movement (REM) stage of sleep.
S, Spier, J, Rivlin, R D, Rowe, T, Egan
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Incidence of the Robin Anomalad (Pierre Robin syndrome)
British Journal of Plastic Surgery, 1983Reliable estimates of the incidence of the Robin Anomalad (Pierre Robin Syndrome) are not readily available in standard texts. An analysis of admissions to the Mersey Regional Cleft Palate Unit (Alder Hey Children's Hospital, Liverpool and the Royal Liverpool Children's Hospital, Heswall) over a 23-year period suggests an incidence of 1:8500 live ...
P G, Bush, A J, Williams
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Laryngeal mask airway guided tracheal intubation in a neonate with the Pierre Robin syndrome
Acta Anaesthesiologica Scandinavica, 1995 Endotracheal intubation in infants with the Pierre Robin syndrome may sometimes be impossible to accomplish by conventional means. To aid difficult tracheal intubation many different techniques have been described.
Tom Hansen
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Nippon Ganka Gakkai zasshi, 1969
PULMONARY hypertension, cardiomegaly, and pulmonary edema have been reported in respiratory obstruction resulting from hypertrophied tonsils and adenoids, and from tracheomalacia in childhood. 1-5 However, these cardiorespiratory changes have not been documented in the respiratory obstruction secondary to the micrognathia and the glossoptosis of the ...
K, Kojima, I, Watanabe, T, Yato
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PULMONARY hypertension, cardiomegaly, and pulmonary edema have been reported in respiratory obstruction resulting from hypertrophied tonsils and adenoids, and from tracheomalacia in childhood. 1-5 However, these cardiorespiratory changes have not been documented in the respiratory obstruction secondary to the micrognathia and the glossoptosis of the ...
K, Kojima, I, Watanabe, T, Yato
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Journal of Pediatric Surgery, 1966
The association of hypoplasia of the mandible with cleft palate and glossoptosis appears to have been first noted by Shukowsky in 1902. However, Pierre Robin in Paris wrote extensively on this association from 1923 onwards and the syndrome has come to bear his name.
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The association of hypoplasia of the mandible with cleft palate and glossoptosis appears to have been first noted by Shukowsky in 1902. However, Pierre Robin in Paris wrote extensively on this association from 1923 onwards and the syndrome has come to bear his name.
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