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Autosomal Recessive Thrombophilia Due to Protein S Deficiency
A protein S deficiency characterized by thrombosis and secondary hemorrhage usually beginning in early infancy that is caused by homozygous or compound heterozygous mutation in the PROS1 gene on chromosome 3q11.1.
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When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
A protein S deficiency characterized by thrombosis and secondary hemorrhage usually beginning in early infancy that is caused by homozygous or compound heterozygous mutation in the PROS1 gene on chromosome 3q11.1.
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