Paciente masculino de 3 meses de edad con diagnostico craneocinostosis + síndrome de pfeiffer + insuficiencia RESPIRATORIA

The current study is given from a purely medical point of view, where the condition of a "3-MONTH-OLDER MALE PATIENT WITH DIAGNOSIS CRANEOCINOSTOSIS + PFEIFFER SYNDROME + RESPIRATORY INSUFFICIENCY" is analyzed, so that among his priorities was knowing the conditions under which the newborn came to the care center. Therefore, in order to establish an appropriate diagnosis and a cure process, or improvement for their disease, the various alternatives to which they could resort and to achieve the expected results were considered. In turn, it was possible to know several considerable factors that helped the decision making and selection of the best option to combat the disease of the newborn. While it is true diseases such as Craneocinostosis, it is a congenital defect within which one or more sutures of the head of a newborn are closed earlier than normal; Its cause is unknown, but certain studies show that genes can be one of them. For its part, Pfeiffer syndrome is a rare and autosomal dominant type of disease that is associated with craniosynostosis. It is a syndrome that affects approximately 1 in 100,000 people. Respiratory failure is nothing more than a disease by which it decreases the oxygen levels in the blood and increases the carbon dioxide levels in a dangerous way. It is important to recognize in time, the various diseases that a newborn can present, since many times it depends on what can be treated at the right time and there are fewer affectations.

• Hlavní autor: Saltos Pazos, Yajaira Cecilia (author)
• Médium: bachelorThesis
• Jazyk: spa
• Vydáno: 2018
• Témata: Craneociostosis; Síndrome de Pfeiffer
• On-line přístup: http://dspace.utb.edu.ec/handle/49000/4482