diseases
Ross Syndrome
Ross syndrome (RS) is a rare disorder of the peripheral autonomic nervous system that is characterized by the triad: tonic pupils, reduced or loss of deep tendon reflexes (hyporeflexia or areflexia), and anhidrosis or hypohidrosis.
Posted September 17, 2022 by Anusha ‐ 2 min read
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PHACE Syndrome
PHACE syndrome is an association between large infantile hemangiomas of the face, head and / or neck and developmental defects of the eyes, heart, major arteries and brain.
Posted September 17, 2022 by Anusha ‐ 2 min read
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Cobb Syndrome
Cobb syndrome is a rare, non-inherited disorder characterized by visible skin lesions with underlying spinal angiomas or arteriovenous malformations (AVM). The skin lesions typically are present as Port-Wine Stains (light pink to dark purple birthmarks), but reports exist of angiokeratomas, angiolipomas, and lymphangioma circumscriptum.
Posted September 17, 2022 by Anusha ‐ 2 min read
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Cloves Syndrome
Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevis, Spinal/Skeletal Anomalies/Scoliosis (CLOVES) syndrome is a very rare congenital (present at birth) disorder characterized by a combination of vascular (involving the blood vessels), skin, spinal, and bone or joint abnormalities.
Posted September 17, 2022 by Anusha ‐ 3 min read
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Crouzon Syndrome
Crouzon syndrome, also known as craniofacial dysostosis, is a complex genetic birth disorder that may affect a child’s face, skull, and teeth. In a child with this syndrome, premature fusion of certain skull bones (craniosynostosis) prevents the skull from growing normally and affects the shape of the head and face; sometimes causing increased pressure around the brain.
Posted September 17, 2022 by Anusha ‐ 3 min read
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