A RARE CAUSE OF NEONATAL HYPOTONIA: FIRST CASE OF AUTOSOMAL RECESSIVE FAST-CHANNEL CONGENITAL MYASTHENIC SYNDROME TYPE 1B IN ALBANIA

A Rare Cause of Neonatal Hypotonia: First Case of Autosomal Recessive Fast-Channel Congenital Myasthenic Syndrome Type 1B in Albania

Hypotonia is a concern, with high morbidity and poor outcomes in 10% of neonatal care cases.Neonatal hypotonia presents a diagnostic challenge for neonatologists, as it may be a sign of a central nervous disorder (hypoxic-ischemic insult, intracranial hemorrhage, cerebral palsy), inborn errors of metabolism, a primary neuromuscular disorder, or a g

read more