What does SRPS mean in SYNDROMES
Short Rib Polydactyly Syndrome (SRPS) is a complex genetic disorder caused by mutations in the genes encoding components of the extracellular matrix. It is associated with multiple malformations such as rib anomalies, polydactyly, and craniofacial and skeletal abnormalities. SRPS has variable presentations and is categorized into three distinct subtypes, each characterized by its own distinctive features. Q&A
SRPS meaning in Syndromes in Medical
SRPS mostly used in an acronym Syndromes in Category Medical that means Short Rib Polydactyly Syndrome
Shorthand: SRPS,
Full Form: Short Rib Polydactyly Syndrome
For more information of "Short Rib Polydactyly Syndrome", see the section below.
Essential Questions and Answers on Short Rib Polydactyly Syndrome in "MEDICAL»SYNDROMES"
What causes SRPS?
SRPS is caused by mutations in the genes encoding components of the extracellular matrix.
What are the symptoms of SRPS?
The symptoms associated with SRPS vary depending on the type of SRPS present, but can include rib anomalies, polydactyly, abnormal facial structure, hydrocephalus, and musculoskeletal abnormalities.
Are there different types of SRPS?
Yes, there are three distinct subtypes of SRPS which are characterized by their own unique features. They include single median maxillary central incisor syndrome (SMMCI), Majewski osteodysplastic primordial dwarfism type II (MOPD II) and short rib-polydactyly syndrome type III (SRPIII).
How is SRPS diagnosed?
Diagnosis of SRPS requires laboratory genetic testing to identify gene mutations that cause this condition. Imaging tests may also be used to confirm diagnosis due to its variable presentation.
Is there any treatment for patients diagnosed with SRP?
While there is no cure for this condition, treatments focus on managing pain, improving quality of life and addressing any complications that arise from this condition such as breathing difficulties or infection due to underdeveloped organs or body parts. Surgery may also be used to correct some deformities associated with this condition such as polydactyly or craniofacial deformities.
Final Words:
SRP is a rare genetic disorder caused by gene mutations resulting in multiple malformations including rib anomalies and polydactyly. Its diagnosis requires laboratory genetic testing and imaging tests to confirm due to its variable presentation. There is no cure for this condition but it can be managed through various treatments such as pain management and surgery for structural abnormalities associated with this condition.
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