- Pierre Robin sequence (syndrome)
- Pi·erre Ro·bin sequence (syndrome) (pyār-ro-băґ) [Pierre Robin, French dentist, 1867–1950] see under sequence.
Medical dictionary. 2011.
Pierre Robin sequence (syndrome)
Look at other dictionaries:
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 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 — Pierre Ro·bin syndrome .pyer rȯ ban n a congenital defect of the face characterized by micrognathia, abnormal smallness of the tongue, cleft palate, and absence of the gag reflex and sometimes accompanied by bilateral eye defects, glaucoma, or… … Medical dictionary
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-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
Syndrome de Stickler — Référence MIM 108300 184840 604841 Transmission Dominante Chromosome 1p21 6p21.3 … Wikipédia en Français
Stickler syndrome — Infobox Disease Name = Stickler syndrome Caption = DiseasesDB = 29327 ICD10 = ICD10|Q|87|8|q|80 ICD9 = ICD9|756.0 ICDO = OMIM = 108300 OMIM mult = OMIM2|277610 OMIM2|184840 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Stickler syndrome … Wikipedia
Catel-Manzke syndrome — Infobox Disease Name = Catel Manzke syndrome Caption = DiseasesDB = 33832 ICD10 = ICD9 = ICDO = OMIM = 302380 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Catel Manzke syndrome is a rare genetic disorder characterized by distinctive… … Wikipedia
Liste de maladies rares — Cette page liste des maladies rares. Sommaire : Haut A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0 9 A Aagenaes, syndrome d … Wikipédia en Français
