Pierre Robin syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29413 ICD10 = ICD10|Q|87|0|q|80 ICD9 = ICDO = OMIM = 261800 MedlinePlus = 001607 eMedicineSubj = ped eMedicineTopic = 2680 eMedicine mult = eMedicine2|ent|150 MeshID = D010855 Pierre Robin… … Wikipedia
Pierre Robin syndrome — a congenital disease in which affected infants have a very small lower jawbone (mandible) and a cleft palate. They are susceptible to feeding and respiratory problems. Pierre Robin (1867 1950), French dentist … Medical dictionary
Pierre Robin syndrome — a congenital disease in which affected infants have a very small lower jawbone (mandible) and a cleft palate. They are susceptible to feeding and respiratory problems. [Pierre Robin (1867–1950), French dentist] … The new mediacal dictionary
Pierre Robin (surgeon) — Pierre Robin (1867 1950) was a French surgeon. [WhoNamedIt|doctor|1233] Pierre Robin syndrome is named for him. [eMedicine|ped|2680] References … Wikipedia
Syndrome de Pierre Robin — Le syndrome de Pierre Robin, ou plus précisément séquence de Pierre Robin, n est pas une maladie mais un groupe de maladies dont les symptômes comprennent au moins la triade oro faciale suivante : Rétrognathisme (menton fuyant) Fente vélo… … Wikipédia en Français
Pierre Robin sequence — the triad of micrognathia, cleft palate, and glossoptosis, with backward and upward displacement of the larynx and angulation of the manubrium sterni; cleft palate makes sucking and swallowing difficult, permitting easy access of fluids into the… … Medical dictionary
Pierre-Robin-Syndrom — Klassifikation nach ICD 10 Q87.0 Angeborene Fehlbildungssyndrome mit vorwiegender Beteiligung des Gesichtes … Deutsch Wikipedia
Pierre-Robin-Sequenz — Klassifikation nach ICD 10 Q87.0 Angeborene Fehlbildungssyndrome mit vorwiegender Beteiligung des Gesichtes … Deutsch Wikipedia
Pierre Robin sequence (syndrome) — Pi·erre Ro·bin sequence (syndrome) (pyār ro băґ) [Pierre Robin, French dentist, 1867–1950] see under sequence … Medical dictionary
síndrome de Pierre-Robin — Eng. Pierre Robin syndrome Síndrome debido a alteraciones del desarrollo fetal que se manifiesta al nacer y cursa con micrognatia, glosoptosis, expresión facial con aspecto de pájaro, microftalmos, protosis, ptosis, miopía magna, glaucoma,… … Diccionario de oftalmología