نتایج جستجو برای: craniofacial anomaly
تعداد نتایج: 46197 فیلتر نتایج به سال:
The occurrence of balanced reciprocal translocation chromosome 1 and 7 is one the rare anomalies. present case report focuses on a 07-year-old male patient with craniofacial anomaly due to manifesting as microcephaly, microstomia, oligodontia scrotal hypospadias bilateral retractile testis. had severe retrognathic hyperdivergent mandible along multiple carious unerupted permanent teeth. After c...
Objectives: Sella turcica is a substantial anatomic reference structure used to assess craniofacial growth and treatment changes in orthodontics. The aim of this retrospective study was analyze the size morphology sella different subdivisions Class II malocclusion compare it I development. Materials Methods: conducted with 150 patient’s pre-treatment lateral cephalometric radiographs. Good-qual...
Tooth development is a highly heritable process which relates to other growth and developmental processes, and which interacts with the development of the entire craniofacial complex. Abnormalities of tooth development are common, with tooth agenesis being the most common developmental anomaly in humans. We performed a genome-wide association study of time to first tooth eruption and number of ...
without significant bone anomalies was unlikely as child did not have affected relatives. There are wide variety of congenital or hereditary disorders in which there is total or partial absence of nails. These disorders are usually associated with other major congenital anomalies. Fetal phenytoin syndrome occurs approximately 7 to 10% of all babies exposed to phenytoin during pregnancy. The fea...
Hemifacial microsomia (HFM) is the most common craniofacial anomaly after cleft lip and cleft palate; this deformity primarily involves the facial skeleton and ear, with either underdevelopment or absence of both components. In patients with HFM, the management of the asymmetries requires a series of treatment phases that focus on their interception and correction, such as distraction osteogene...
Upper airway resistant syndrome (UARS) is more common in children than is obstructive sleep apnea syndrome (OSAS). Age will color the symptoms associated with the syndrome. UARS must be looked for in families with adult sleep-disordered breathing. Polygraphic recording during sleep will show flow limitation with usage of nasal cannula/pressure transducer system, but the abnormal breathing durin...
Rieger syndrome is a dysembryogenetic disease in which labyrinthic damage can be associated with other genetic anomalies. The case presented here is of a patient who has bilateral dysgenesis of the iris, with bulbar atrophy and dyscoria. The patient does not present any malformation of the craniofacial structures, of the periumbilical skin, or of the skeletal bones. The case is, therefore, a va...
Morning glory syndrome (MGS) is a rare congenital optic disc anomaly characterized by a funnel-shaped, excavated optic disc surrounded by chorioretinal pigmentary disturbance. The main ophthalomoscopic feature of the MGS is enlarged optic disc with a funnel shaped scleral defect; elevated peripapillary chorioretinal pigmentation; and pale fluffy tissue of glial hyperplasia overlying the optic d...
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