نتایج جستجو برای: median cleft

تعداد نتایج: 161927  

2015
Nikolaos Gkantidis Despina A Papamanou Marina Karamolegkou Domna Dorotheou

OBJECTIVES To evaluate the level of satisfaction of individuals with cleft lip and/or palate (CLP) and their parents concerning the esthetic and functional treatment outcomes, the impact of the cleft on everyday life, and potential associations with treatment outcome satisfaction. SUBJECTS AND METHODS The sample consisted of 33 patients (7 CP, 20 unilateral CLP, and 6 bilateral CLP; median ag...

Journal: :The Journal of craniofacial surgery 2009
Arun K Gosain Amir H Fathi

BACKGROUND Secondary rhinoplasty after a cleft lip repair remains a significant challenge. We have developed a technique in which resorbable plates are used to support the cleft alar cartilage to minimize relapse. There are few guidelines by which one can objectively assess the outcome of cleft rhinoplasty over time. This study attempts to demonstrate a means by which the symmetry and form of t...

Journal: :Thorax 1980
R K Firmin L S Fragomeni S C Lennox

A case of complete cleft sternum is presented along with the nomenclature of sternal defects. It is recommended that the term ectopia cordis should be applied only to cases in which the heart and thoracic viscera are genuinely ectopic. Surgical correction of complete cleft sternum should be performed in the neonatal period whether the infant is symptomatic or not. Simple closure of the defect, ...

Journal: :avicenna journal of medical biotechnology 0

background: the purpose of this study was to describe the association of mthfr gene single nucleotide polymorphisms (c677t and a1298c) and maternal supplementary folate intake with orofacial clefts in the iranian population. methods: in this case-control study, peripheral venous blood was taken from 65 patients with orofacial clefts and 215 unaffected controls for dna extraction and kept in edt...

Journal: :Case Reports in Perinatal Medicine 2022

Abstract Objectives Hamartomas are non-neoplastic developmental anomalies, mostly congenital, characterized by uncontrolled, disorganized proliferation of local endogenous tissue, which can normally be found at the site origin and very often mesodermally derived. It is well known that hamartoma associated with congenital midline cervical cleft therefore cause a variety symptoms. In general, the...

2016
Chima Oji

We present the case of a newborn with a rare combination of trifid tongue, macroglossia, ankyloglossia, median cleft of the lower lip, bony Tumour on the mandible and cleft of the palate. Our surgical procedure consisted in the release and repair of the trifid tongue; removal of the Tumour on the mandible and repair of the cleft of the lower lip. Finally, we carried out a novel technique to red...

Journal: :The Canadian journal of plastic surgery = Journal canadien de chirurgie plastique 2007
Craig Stewart Lowell A Hughes Hugh G Thomson Derek Armstrong Vito Forte

True median cleft of the upper and lower lip occurs very rarely. Complete or partial facial duplication is an extremely rare malformation. Approximately 26 cases have been reported since 1900, spanning a wide spectrum of clinical severity. Most cases appear to share a number of features, including cleft palate, duplication of the tongue, orbital hypertelorism and macrostomia. An unusual patient...

2013
Sondos Abuzinada Ahmed Alyamani

Purpose: To evaluate the skeletal changes associated with maxillary advancement using the external rigid distractor in cleft lip and palate patients after distraction and to assess the stability of these changes. Patients and Methods: Eight cleft lip and palate patients with maxillary hypoplasia underwent maxillary distraction osteogenesis using external rigid devise. Lateral cephalometric reco...

Journal: :journal of family and reproductive health 0
ilana naghi department of obstetrics and gynecology, shahid beheshti university of medical sciences, tehran, iran. babak behnam department of medical genetics, tehran university of medical sciences.

a 39-year-old pregnant woman at 38 weeks of gestation was referred with labor pain to a hospital. she had consanguinity with her husband. a female newborn had multiple craniofacial anomalies and phocomelia in right upper limb. the disease locus was assigned to chromosome17q21. four days later, infant died of cardiopulmonary arrest.

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