Background and Purpose. Children often are referred for physical therapy with the diagnosis of hypotonia when the definitive cause of hypotonia is unknown. The purpose of this case report is to describe the clinical decision-making process using the Hypothesis-Oriented Algorithm for Clinicians II (HOAC II) for an infant with hypotonia and gross motor delay. Case Description. The patient was a 5-month-old infant who had been evalu-ated by a neurologist and then referred for physical therapy by his pediatrician. Physical therapy evaluation results and clinical observations of marked hypotonia, significant gross motor delay, tongue fasciculations, feeding difficulties, and respira-tory abnormalities prompted necessary referral to specialists. ...
Background The advent of new therapies has increased the need to achieve early diagnosis in Spinal M...
The disorder is found in infants, and not many people heard of this disability. People need to be in...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by degen...
Background and Purpose. Children often are referred for physical therapy with the diagnosis of hypot...
Background: Spinal Muscular Atrophy (SMA) is an autosomal recessive neuromuscular condition characte...
Introduction: Spinal Muscular Atrophy (SMA) is a progressive neuromuscular disease causing degenerat...
The differential diagnosis of neonatal hypotonia is a complex task, as in newborns hypotonia can be ...
Background: Infantile hereditary proximal spinal muscular atrophy (SMA) type 1 is characterized by o...
Background and Purpose: Developmental delay is a common condition seen in the pediatric populations ...
Background and purpose: This case report describes a physical therapy program that included foot ort...
BACKGROUND:The advent of new therapies has increased the need to achieve early diagnosis in Spinal M...
Congenital hypotonia with favorable outcome is characterized by an early neonatal onset and a benign...
Introduction Myotonic dystrophy (MD) is a neuromuscular disease and is characterized by myotonia in ...
The diagnosis of severe type 1 spinal muscular atrophy (SMA) should be confirmed by an expert in pae...
AbstractBackgroundSpinal muscular atrophy is a rare genetic disease with devastating neurodegenerati...
Background The advent of new therapies has increased the need to achieve early diagnosis in Spinal M...
The disorder is found in infants, and not many people heard of this disability. People need to be in...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by degen...
Background and Purpose. Children often are referred for physical therapy with the diagnosis of hypot...
Background: Spinal Muscular Atrophy (SMA) is an autosomal recessive neuromuscular condition characte...
Introduction: Spinal Muscular Atrophy (SMA) is a progressive neuromuscular disease causing degenerat...
The differential diagnosis of neonatal hypotonia is a complex task, as in newborns hypotonia can be ...
Background: Infantile hereditary proximal spinal muscular atrophy (SMA) type 1 is characterized by o...
Background and Purpose: Developmental delay is a common condition seen in the pediatric populations ...
Background and purpose: This case report describes a physical therapy program that included foot ort...
BACKGROUND:The advent of new therapies has increased the need to achieve early diagnosis in Spinal M...
Congenital hypotonia with favorable outcome is characterized by an early neonatal onset and a benign...
Introduction Myotonic dystrophy (MD) is a neuromuscular disease and is characterized by myotonia in ...
The diagnosis of severe type 1 spinal muscular atrophy (SMA) should be confirmed by an expert in pae...
AbstractBackgroundSpinal muscular atrophy is a rare genetic disease with devastating neurodegenerati...
Background The advent of new therapies has increased the need to achieve early diagnosis in Spinal M...
The disorder is found in infants, and not many people heard of this disability. People need to be in...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by degen...