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Proteus syndrome is a rare genetic disorder [1] that can cause tissue overgrowth involving all three embryonic lineages. Patients with Proteus syndrome tend to have an increased risk of embryonic tumor development. [2] The clinical symptoms and radiographic findings of Proteus syndrome are highly variable, as are its orthopedic manifestations ...
The disease belongs to a family of hamartomatous polyposis syndromes, which also includes Peutz–Jeghers syndrome, juvenile polyposis and Cowden syndrome. Mutation of the PTEN gene underlies this syndrome, as well as Cowden syndrome, Proteus syndrome, and Proteus-like syndrome, these four syndromes are referred to as PTEN Hamartoma-Tumor ...
Children with some overgrowth syndromes such as Klippel–Trénaunay syndrome can be readily detectable at birth. [3] In contrast, other overgrowth syndromes such as Proteus syndrome usually present in the postnatal period, characteristically between the second and third year of life. [ 2 ]
Sellars was born with abnormally large and misshapen legs and feet, which continued to grow at a disproportionate rate. In a November 2009 interview, she estimated that she weighed about 21 stone (294 lb or 133 kg): 6 stone (84 lb or 38 kg) for her upper body and the remainder in her legs and feet (210 lb or 95 kg).
Pronator teres syndrome; Propofol infusion syndrome; Proteus syndrome; Proteus-like syndrome; Prune belly syndrome; Pseudo-Cushing's syndrome; Pseudodementia; Pseudoexfoliation syndrome; Psychoorganic syndrome; Puer aeternus; Pulmonary-renal syndrome; Purple glove syndrome; Purple urine bag syndrome
Proteus-like syndrome (PLS) is a condition similar to Proteus syndrome, but with an uncertain cause. [1] It's characterized by skeletal and hamartous overgrowth of multiple tissues, nevi in cerebriform connective tissue, blood vessel malformations and linear epidermal nevi.
Multiple hamartoma syndrome is a syndrome characterized by more than one hamartoma. [1]: 673 It is sometimes equated with Cowden syndrome. However, MeSH also includes Bannayan–Zonana syndrome (that is, Bannayan–Riley–Ruvalcaba syndrome) and Lhermitte–Duclos disease under this description.
Cohen was born in Boston, Massachusetts, and studied at the University of Michigan, Tufts University, the University of Minnesota, and Boston University.His post-graduate training included a fellowship in pathology and medical genetics with Robert Gorlin (1923–2006), an oral pathologist and geneticist who described a large number of syndromes, including one they delineated together known as ...