Sökning: "Congenital"

Visar resultat 1 - 5 av 369 avhandlingar innehållade ordet Congenital.

1. 1. Congenital clubfoot : Aspects on epidemiology, residual deformity and patient reported outcome

   Författare :Henrik M Wallander; Göran Hansson; Sune Larsson; Michael Benson; Uppsala universitet; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Congenital clubfoot; incidence; ultrasonography; forefoot adduction; navicular position; spurious correction; Ilizarov External Fixator; subjective outcome; stiffness; patient reported outcome; norm group; gender difference; Orthopaedics; Ortopedi; Orthopaedics; ortopedi;

   Sammanfattning : The overall aim of this thesis on congenital clubfoot was to estimate the incidence with a national perspective, analyse residual deformities and their management, and evaluate patient reported long-term quality of life and foot function. Paper I was a prospective, nationwide sampling of 280 children with congenital clubfoot during 1995-96. LÄS MER

3. 2. Congenital muscular torticollis

   Författare :Anna Öhman; Göteborgs universitet; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; congenital muscular torticollis; infant; neck ROM;

   Sammanfattning : Congenital Muscular torticollis Anna Öhman. Institute of Neuroscience and Physiology, Division of Physical Therapy, Sahlgrenska Academy at Göteborg University, Göteborg, Sweden. LÄS MER

4. 3. Congenital Recessive Ichthyosis : Studies of Gene Expressions Related to Keratinocyte Differentiation and Skin Barrier Repair

   Författare :Hanqian Zhang; Hans Törmä; Anders Vahlquist; Marie Virtanen; Mikael Ivarsson; Uppsala universitet; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; genodermatoses; oligoarray; trancriptomics; transglutaminase-1; cornified envelope; peroxisome proliferator-activated receptor δ; all-trans retinoic acids.; Dermatologi och venereologi; Dermatology and Venerology;

   Sammanfattning : Autosomal recessive congenital ichthyosis (ARCI) is a rare monogenetic disorder characterized by a defective skin barrier, hyperkeratosis, and dry, scaly skin. It affects keratinocyte differentiation and is caused by mutations in any of at least 12 genes believed to control the formation of ω-O-acylceramide and the corneocyte lipid envelope (CLE): ABCA12, ALOXE3, ALOX12B, CERS3, CYP4F22, ELOVL4, LIPN, NIPAL4, PNPLA1, SDR9C7, SLC27A4, and TGM1. LÄS MER

5. 4. Congenital muscular torticollis

   Författare :Anna Öhman; Göteborgs universitet; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; craniofacial asymmetry; rotation; lateral flexion; muscle function; infants; reference values; torticollis; early motor milestones; stretching treatment; physiotherapy;

   Sammanfattning : Aim: The purpose of these studies was to undertake a survey of functional and cosmetic status in children treated for congenital muscular torticollis (CMT), to examine validity and reliability of the Muscle Function Scale (MFS), to find reference values for rotation and lateral flexion of the neck and muscle function of the lateral flexors in the neck for the normally developing infant, to investigate if infants with CMT are at higher risk of achieving the early motor milestones later compared to a control group of healthy infants and to investigate if treatment duration is affected when stretching is carried out by an experienced physiotherapist compared to parents. Methods: Range of motion (ROM) in neck rotation was measured with an arthrodial protractor. LÄS MER

7. 5. Management of Adults with Congenital Heart Disease

   Författare :Daniel Samarai; Kardiologi; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Adults with Congenital Heart Disease; Congenital Heart Disease; Congenital heart defect CHD ; Anticoagulation; Anticoagulants; anticoagulant treatment; Thromboembolic events; Major bleeding; Diagnostic Imaging methods;

   Sammanfattning : Adults with congenital heart disease (ACHD) are a completely new and rapidly growing specialty comprising patients who require specialist knowledge regarding their care and treatment. Challenges involve diagnostics and treatment as studies are scarce and include small and heterogenous study populations. LÄS MER