Severe combined immunodeficiency diagnosis and genetic defects.

Severe combined immunodeficiency (SCID) is a rare and life-threatening genetic disorder that severely impairs the immune system's ability to defend the body against infections. Often referred to as the "bubble boy" disease, SCID gained widespread recognition due to the case of David Vetter, a young boy who lived in a sterile plastic bubble to protect him from germs. SCID is typically present at birth, and it results from genetic mutations that affect the development and function of immune cells, particularly T cells and B cells. These immune cells are essential for identifying and fighting off infections caused by viruses, bacteria, and fungi. In SCID patients, the immune system is virtually non-existent, leaving them highly susceptible to recurrent, severe infections. There are several forms of SCID, with varying degrees of severity, but all share common features. Newborns with SCID often exhibit symptoms such as chronic diarrhea, thrush, skin rashes, and persistent infections that do not respond to standard treatments. Without prompt diagnosis and intervention, SCID can lead to life-threatening complications and a high risk of mortality. There are over 20 possible affected genes. Treatment options for SCID primarily involve immune reconstitution, with the most well-known approach being hematopoietic stem cell transplantation (HSCT). Alternatively, gene therapy is also available for some forms of SCID. Once treated successfully, SCID patients can lead relatively normal lives, but they may still require vigilant infection control measures and lifelong medical follow-up to manage potential complications. In conclusion, severe combined immunodeficiency is a rare but life-threatening genetic disorder that severely compromises the immune system's function, rendering affected individuals highly vulnerable to infections. Early diagnosis and appropriate treatment are fundamental. With this respect, newborn screening is progressively and dramatically improving the prognosis of SCID.

Hiperglicinemia näo cetótica / Nonketotic hyperglycinemia

A hiperglicinemia näo cetótica é considerada um erro inato do metabolismo que causa sérias seqüelas neurológicas no lactente, podendo levar ao coma e à morte, principalmente no período neonatal. Os autores descrevem o caso de uma menina de 7 meses de vida com hipotonia, letargia, convulsöes de difícil controle e coma. O diagnóstico foi confirmado pela cromatografia quantiativa de aminoácidos no sangue, no líquor e na urina, que demonstraram altos níveis de glicina näo degradada.As dificuldades terapêuticas säo consideradas. Os autores também salientam a importância deste diagnóstico como causa de lesäo cerebral, que tem implicaçöes tanto no cuidado do paciente, quanto no aconselhamento genético.(au)