نتایج جستجو برای: philtrum
تعداد نتایج: 262 فیلتر نتایج به سال:
Aims and objectives: Facial morphology is influenced by both genetic and environmental factors which interact in complex ways to determine the form and function of the craniofacial complex. Many studies have been done to know the amount of heritability of the skeletal components but hardly are known about the heritability of soft tissue pattern which is compared by everyone as soon as the child...
Riya George1, MD; Fehmida Najmuddin*2, MD; Rajesh Rai2, MD; Keya Lahiri2, DCH, MD 1Department of Pediatrics, KJ Somaiya Medical College, 2DY Patil Medical College, Hospital & Research Centre, India Received: Apr 15, 2014; Accepted: Aug 19, 2014; Online Available: Sep 10, 2014 Trichorhinophalangeal syndrome (TRPS), as the name suggests is a rare genetic disorder which affects the tricho (hair), ...
Facial morphology measurement and classification play important role in the face anthropometry of many medical applications. This usually involves the investigation of medical abnormalities where specific facial features are studied by taking a number of measurements of the facial area under investigation. The measurements are often obtained from the threedimensional (3D) scans of the faces; ho...
Background: Cornelia de Lange syndrome (CdLS) is a genetic disorder featured by multi-systemic malformations, such as microcephaly, hypertrichosis, upper limb defects, growth retardation, developmental delay, and variety of associated malformations. Multidisciplinary holistic care needed in the management rehabilitation individuals with CdLS. One tools that can be used clinical measurement Inte...
A CASE REPORT: UNILATERAL COMPLETE CLEFT LIP RECONSTRUCTION USING THE MODIFICATION MILLARD TECHNIQUE
Highlights: The modified Millard technique, including the Tennison triangular flap, is effective in preventing vermillion notching and reducing scar complications cleft lip repairs. technique addresses concerns related to compromised tissue nostril deformities, leading improved appearance functionality. Scar thinning techniques separate nasoraphy contribute enhanced aesthetics optimal healing A...
Williams syndrome (WS), also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by infantile hypercalcemia, short stature, varying degree of mental retardation, elfin-like facial features, and cardiovascular abnormalities, including systemic hypertension, aortic hypoplasia, coarctation the aorta, valvular heart disease (aortic pulmonic stenosis, mitral valve prolapsed o...
Background: X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder, in which patients present with lissencephaly, agenesis of the corpus callosum, refractory epilepsy of neonatal onset, acquired microcephaly, and male genotype with ambiguous genitalia. XLAG is responsible for a severe neurological disorder of neonatal onset in boys. A gyration defect con...
Background Monosomy is defined as the presence of only one chromosome instead of two in humans. Partial monosomy occurs when only a portion of the chromosome is present in a single copy, while the rest has two copies. It can occur in unbalanced translocations or deletions. Case report In this report, a 6 years old girl was presented who was referred to the Pediatric Dep, Shahid Sadoughi Ho...
BACKGROUND Monosomy is defined as the presence of only one chromosome instead of two in humans. Partial monosomy occurs when only a portion of the chromosome is present in a single copy, while the rest has two copies. It can occur in unbalanced translocations or deletions. CASE REPORT In this report, a 6 years old girl was presented who was referred to the Pediatric Dep, Shahid Sadoughi Hospi...
Hypohidrotic ectodermal dysplasia (HED) is the most prevalent type of ectodermal dysplasia (ED). ED is an umbrella term for a group of syndromes characterized by missing or malformed ectodermal structures, including skin, hair, sweat glands, and teeth. The X-linked recessive (XL), autosomal recessive (AR), and autosomal dominant (AD) types of HED are caused by mutations in the genes encoding ec...
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