Debunking the Myth: Should Pierre Robin be Credited for Defining the Pierre Robin Sequence?

被引：0

作者：

Leger, Maelys ^{[1
,2
]}

Baudouin, Robin ^{[3
,4
]}

Thierry, Briac ^{[1
,2
]}

机构：

[1] Necker Enfants Malad Hosp, AP HP, Dept Pediat Otolaryngol, Paris, France

[2] Paris Cite Univ, Sch Med, ENT Dept, Paris, France

[3] Foch Hosp, Dept Otolaryngol Head & Neck Surg, Suresnes, France

[4] Paris Saclay Univ, UFR Simone Veil Versailles St Quentin En Yvelines, Lab Anthropol Archaeol Biol LAAB, Montigny Le Bretonneux, France

来源：

OTOLARYNGOLOGY-HEAD AND NECK SURGERY | 2025年 / 172卷 / 03期

关键词：

airway obstruction; cleft palate; congenital; glossoptosis; pediatrics; Pierre Robin syndrome; retrognathia;

D O I：

10.1002/ohn.1064

中图分类号：

R76 [耳鼻咽喉科学];

学科分类号：

100213 ;

摘要：

The Pierre Robin Sequence is a rare craniofacial malformation that invariably combines retrognathism, glossoptosis, and upper airway obstruction, with a prevalence ranging from 1 in 8000 to 1 in 14,000 newborns. Although formally described by the French physician Pierre Robin in 1923, older and even ancient as far back as the Babylonian times, descriptions have been identified. Dr Pierre Robin's perspicacity lay in putting up a treatment for the patients presenting those symptoms. That is why his successors honored his work by naming this disease after him.

引用

页码：1114 / 1117

页数：4

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