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1,402 Possible Causes for 3, cleft, orofacial

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  • Osteoporosis

    The main features of this autosomal inherited disease are ocular, auditory with orofacial abnormalities and early-onset osteoarthritis.[] Potter MDE 1, 2, 3 , Walker MM 4, 5 , Hancock S 6 , Holliday E 7 , Brogan G 8, 9 , Jones M 10 , McEvoy M 11 , Boyle M 12, 13 , Talley NJ 14, 15, 16 , Attia J 17, 18 .[] Haploinsufficiency of SATB2 causes cleft palate, intellectual disability with deficient speech, facial and dental abnormalities, and other variable features known collectively[]

  • Cyclic Neutropenia

    […] cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial[] Gingivitis Stomatitis Bacterial infections The diagnosis of cyclic neutropenia is made through continuous monitoring, noting neutropenia of 200 neutrophils/microL on at least 3-[] There is no case in the literature that has reported the presence of cyclic neutropenia in cleft patients.[]

  • Non-Syndromic Orofacial Cleft

    The aim of this study was to investigate associations between genetic variants of FOXE1 and risk of non-syndromic orofacial clefts in a Chinese population.[] […] for oral clefts, and describe treatments by the various professionals of the cleft team.[] Li D 1, 2 , Zhang H 3 , Ma L 1, 2 , Han Y 1, 2 , Xu M 1, 2 , Wang Z 1, 2 , Jiang H 1, 2 , Zhang W 1, 2 , Wang L 1, 2 , Pan Y 1, 2 .[]

  • Amoxicillin

    Huddinge, Sweden. 3 Department of Laboratory Medicine, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden. 4 Department of Dental Medicine, Division of Orofacial[] Ariza A 1 , Mayorga C 1, 2, 3 , Salas M 2 , Doña I 2 , Martín-Serrano Á 1, 3 , Pérez-Inestrosa E 3, 4 , Pérez-Sala D 5 , Guzmán AE 6 , Montañez MI 1, 3 , Torres MJ 2, 3 .[] Synthesis, characterization and molecular recognition properties of fluorene based supramolecular cleft 1 is reported.[]

  • Angelman Syndrome

    The aim of this paper is to present three cases of AS, reporting the orofacial characteristics and requisite dental care in these patients.[] Banko J 1, 3 , Lussier AL 1, 2 , Weeber EJ 1, 2 .[] A child with Angelman syndrome, cutis aplasia, cleft palate, and congenital microform cleft lip, born to a father with a Robertsonian translocation 13;15 is described.[]

  • Tolosa-Hunt Syndrome

    OROFACIAL PAIN AND HEADACHE is a timely, comprehensive and instructive addition to the pain literature; in particular the important and truly multidisciplinary area of orofacial[] […] editions of International Classification of Headache Disorders (ICHD) diagnostic criteria for Tolosa-Hunt syndrome (THS) have been published in 1988, 2004 and 2013, in ICHD-3[] A ruptured Rathke's cleft cyst (RCC) was identified within the adenohypophysis, with a chronic inflammatory reaction in surrounding pituitary and overlying hypothalamus.[]

  • Phenylketonuria

    ., orofacial clefting and bladder exstrophy)--a condition known as maternal PKU syndrome.[] CASE PRESENTATION: We report a case of a 3 year- old boy affected by classic PKU and FD, both confirmed by molecular data.[] ., orofacial clefting and bladder exstrophy)--a condition known as maternal PKU syndrome.[]

  • Osteogenesis Imperfecta

    BACKGROUND: Osteogenesis Imperfecta (OI) is characterized by a number of deviations in the orofacial region.[] Tonight, you'll meet Destiny and Tiffany, both 21, who have Osteogenesis Imperfecta Type 3.[] The radiologic images revealed such anomalies and variations as a cleft palate, mandibular dysplasia, spina bifida, costa cervicalis, and fusion of the ribs and vertebrae,[]

  • Anesthetic

    BACKGROUND: To compare the analgesic effect of anesthetic infiltration of lidocaine 2% and low-level laser therapy (LLLT) by GaAlAs into tender points of patients with orofacial[] LAST cases were identified based on MedDRA system organ classes (Approach 1), a recent publication (Approach 2), and a novel approach based on LAST literature (Approach 3)[] Acostello et al further classify cleft sternum into complete or partial (superior, medium, inferior) with a simple superior partial cleft sternum being by far the most common[]

  • Noma

    This case report describes a baby with noma, an orofacial gangrenous infection.[] Trop Doct. 2018 Jul;48(3):230-232. doi: 10.1177/0049475518754720. Epub 2018 Jan 25.[] By comparing large numbers of noma patients and cleft lip patients in a large referral hospital for these disorders in Sokoto, Nigeria, we calculated the incidence of noma[]