نتایج جستجو برای: alopecia totalis
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Situs inversus totalis is a rare congenital anomaly characterized by the mirror-image position of abdominal and thoracic organs, heart compared to their normal anatomical position. The estimated prevalence situs in general population ranges from 1:6500 1:25000. can be associated with primary ciliary dyskinesia, structural abnormalities heart, anomalies visceral clinical picture depends on anoma...
262 Ann Dermatol Received Setember 21, 2012, Revised February 21, 2013, Accepted for publication April 22, 2013 Corresponding author: Sook-Ja Son, Department of Dermatology, Eulji General Hospital, 68 Hangeulbiseong-ro, Nowon-gu, Seoul 139-711, Korea. Tel: 82-2-970-8580, Fax: 82-2-974-1577, E-mail: ssjmdderma@ daum.net This is an Open Access article distributed under the terms of the Creative C...
Congenital diaphragmatic hernia is a relatively rare disorder (1:3000 newborns) that frequently presents with respiratory distress in the immediate neonatal period due to severe pulmonary hypertension and lung hypoplasia. Extracorporeal membrane oxygenation (ECMO) can be used as a last resort when artificial ventilation and/or modulation of the pulmonary vascular tone fail to improve the clinic...
FOXN1 deficiency is a primary immunodeficiency characterized by athymia, alopecia totalis, and nail dystrophy. Two infants with FOXN1 deficiency were transplanted with cultured postnatal thymus tissue. Subject 1 presented with disseminated Bacillus Calmette-Guérin infection and oligoclonal T cells with no naive markers. Subject 2 had respiratory failure, human herpes virus 6 infection, cytopeni...
BACKGROUND Inositol 1,4,5trisphosphate (IP(3)) and diacylglycerol (DAG) are important intracellular signalling molecules in various tissues. They are generated by the phospholipase C family of enzymes, of which phospholipase C delta (PLCD) forms one class. Studies with functional inactivation of Plcd isozyme encoding genes in mice have revealed that loss of both Plcd1 and Plcd3 causes early emb...
Situs inversus totalis is a rare congenital disorder where the heart being a mirror image is situated on the right side of the body. Distorted cardiac anatomy makes fluoroscopy-guided percutaneous mitral valvotomy (PMV) technically challenging and there are only few reports of PMV in situs inversus totalis. Here we report a case where PMV was successfully done for situs inversus totalis with ra...
To cite: Lakshman VB, Revannasiddaiah S, Ganganna R. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013008611 DESCRIPTION Situs inversus totalis is a rare occurrence wherein the organs of an individual are ‘mirrored’ in position, with the right-sided organs swapping positions with the left. The thorax features the heart placed in the right hemithorax, with the l...
PATIENT Female, 68 FINAL DIAGNOSIS: Gallbladder agenesis with situs inversus totalis Symptoms: Epigastric pain • jaundice MEDICATION - Clinical Procedure: - Specialty: Surgery. OBJECTIVE Rare disease. BACKGROUND Situs inversus totalis is an inherited condition characterized by the mirror-image transposition of thoracic and abdominal organs. Gallbladder agenesis, which has normal bile duct...
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