Congenital atrichia associated with situs inversus and mesocardia
نویسندگان
چکیده
منابع مشابه
Congenital diaphragmatic hernia and situs inversus totalis.
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...
متن کاملSingle coronary artery with mesocardia, situs inversus, and atrioventricular and ventriculoarterial discordance.
a Serviço Diagnóstico por Imagem, Hospital Particular de Viana do Castelo, Viana do Castelo, Portugal e Serviço de Imagiologia, Clínica Girassol, Luanda, Angola b Serviço de Cardiologia Pediátrica, Hospital da Cruz Vermelha, Lisboa, Portugal e Serviço de Cardiologia Pediátrica, Clínica Girassol, Luanda, Angola c Serviço de Cardiologia, Hospital Militar Principal de Luanda, Luanda, Angola d Serv...
متن کاملCongenital aglossia with situs inversus totalis--a case report.
Hypoglassia or aglossia is an uncommon anomaly, either of which may occur as an isolated finding or in association with other deformations, especially limb anomalies. Their genetic background is uncertain, and drug induced teratogen has not been clearly identified. We experienced a case of congenital aglossia with situs inversus in a female infant aged twelve days. Her initial complaints at adm...
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ENDOCARDIAL thickening may be due to a variety of causes, among which are primary myocardial lesions, hypertension, congenital anomalies of the coronary arteries, developmental cardiac defects1-3 beriberi heart disease,4 progressive systemic sclerosis,5 and idiopathic eardiae hypertrophy.i9 Many etiologic factors have been proposed as causative in endocardial fibrosis ;1O these include metaboli...
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ژورنال
عنوان ژورنال: International Journal of Trichology
سال: 2012
ISSN: 0974-7753
DOI: 10.4103/0974-7753.100093