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Autosomal recessive distal spinal muscular atrophy 1

MONDO:0011436

Spinal muscular atrophy with respiratory distress type 1 is a rare genetic motor neuron disease characterized by severe respiratory distress/respiratory failure in association with diaphragmatic eventration and palsy, as well as progressive, symmetrical, distal-to-proximal muscle weakness and atrophy (in lower limbs especially). Patients typically have a history of intrauterine growth retardation, low birth weight, feeble cry, weak suck and failure to thrive and present with inspiratory stridor, recurrent episodes of dyspnea or apnea, cyanosis and absent deep tendon reflexes. Kyphosis/scoliosis, foot deformities and joint contractures are frequently associated features.

Also known as: DSMA1, IGHMBP2 spinal muscular atrophy, SIANRF, SMARD1, Spinal Muscular Atrophy with Respiratory Distress, autosomal recessive distal spinal muscular atrophy 1, autosomal recessive distal spinal muscular atrophy type 1, autosomal recessive spinal muscular atrophy with respiratory distress

30 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Peripheral nervous system disorder (107) Neuromuscular disease (98) Central nervous system disorder (97) Spinal muscular atrophy (93) Peripheral neuropathy (90) Motor neuron disorder (59)
Trials to join now! 18 Not yet recruiting 2 Not yet finished but already full! 4 Completed 6
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