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Muenke syndrome, also known as FGFR3-related craniosynostosis,[1] is a human specific condition characterized by the premature closure of certain bones of the skull during development, which affects the shape of the head and face. Medical genetics is the branch of medicine that involves the diagnosis and management of hereditary disorders. This is a list of diseases starting with the letter "C". Member feedback about Boomerang dysplasia: Presentation This condition is a skeletal dysplasia characterized by short stature, mild brachydactyly, kyphoscoliosis, abnormal gait, enlarged knee joints, precocious osteoarthropathy, platyspondyly, delayed epiphyseal ossification, mild metaphyseal abnormalities, short stature and short and bowed legs.

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Pseudopseudohypoparathyroidism topic Pseudopseudohypoparathyroidism PPHP is an inherited disorder,[1] named for its similarity to pseudohypoparathyroidism in presentation. The Laws of Scientific Hand Reading. Blood levels of parathyroid hormone are elevated in pseudohypoparathyroidism due to the hypocalcemia Genetics This condition is associated with genetic imprinting. This site was created by award-winning author Holly Tuckerwho also served as Editor-in-Chief, and ran for over 9 years Member feedback about Sugarman syndrome:

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Brachydactyly type D | Revolvy

Fitzsimmons—Guilbert syndrome is an extremely rare genetic disease characterized by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal—phalangeal pattern profile, sternal anomaly pectus carinatum or excavatum , dysarthria, and mild intellectual deficit. This is a list of diseases starting with the letter "E". Depending on the level of severity, some individuals with SCS may require some form of medical or surgical intervention.

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