Cutis Gyrata Syndrome of Beare and Stevenson < Genetic Disorders & Chromosomal Abnormalities << Diseases <<< Sick Care Systems (Health Care Systems) @ Wellness Advocate . com

^⌊Genetic Disorders & Chromosomal Abnormalities

^⌊Cutis Gyrata Syndrome of Beare and Stevenson

Genetic Disorders & Chromosomal Abnormalities
^⌊	Rare Genetic Disorders
^⌊	Chromatin Diseases
^⌊	Chromosomal Health Challenges
^⌊	Genetic Imprint Disorders
^⌊	Ciliopathies (Ciliopathy)
^⌊	Contiguous Genes Syndrome
^⌊	X-Linked Dominant Disorders
^⌊	Oculodentodigital Dysplasia (Oculodentodigital Syndrome)
^⌊	Rozin Hertz Goodman Syndrome
^⌊	Bart's Syndrome
^⌊	Worth Syndrome
^⌊	Wisconsin Syndrome
^⌊	Jackson-Weiss Syndrome
^⌊	Rombo Syndrome
^⌊	Unclassified Genetic Disorders

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Cutis Gyrata Syndrome of Beare and Stevenson

“Beare-Stevenson Cutis Gyrata Syndrome”

Cutis Gyrata Syndrome of Beare and Stevenson
In our body, the dis-order, Beare-Stevenson Cutis Gyrata Syndrome is a craniosynostosic dis-order indicative to a specific set of signs, symptoms or other health indicators, associated with a health challenge, involving mutations in the FGFR2 gene. *

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References:
Tartaglia M. et al "Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders" Hum Genet. 1997 Nov;101(1):47-50

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Cutis Gyrata Syndrome of Beare and Stevenson

Cutis Gyrata Syndrome of Beare and Stevenson

References: