"' Cutis marmorata telangiectatica congenita "'or "'CMTC "'is a rare congenital vascular disorder that usually manifests in affecting the blood vessels of the skin.
32.
Alternative names for De Barsy syndrome include corneal clouding-cutis laxa-mental retardation, cutis laxa-growth deficiency syndrome, De Barsy Moens Diercks syndrome, and progeroid syndrome of De Barsy.
33.
Alternative names for De Barsy syndrome include corneal clouding-cutis laxa-mental retardation, cutis laxa-growth deficiency syndrome, De Barsy Moens Diercks syndrome, and progeroid syndrome of De Barsy.
34.
But perhaps the most notable feature, differentiating GO from WSS and similar cutis laxa disorders, is the age-specific metaphyseal peg sometimes found in GO-affected long bone, near the knee.
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Cutis marmorata telangiectatica congenita is clinically similar, but the lesions are more intense, may be segmental, are persistent, and may be associated with loss of dermal tissue, epidermal atrophy and ulceration.
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Additional signs and symptoms of Beare Stevenson cutis gyrata syndrome can include a blockage of the nasal passages ( choanal atresia ), overgrowth of the umbilical stump, and abnormalities of the genitalia and anus.
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The name " Mollicutes " is derived from the Latin mollis ( soft ) and cutis ( skin ), and all of these bacteria do lack a cell wall and the genetic capability to synthesize peptidoglycan.
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The 14 costumes were designed by a California couturier named Ruthie West, who was also the stylist for the Jackson 5, Thelma Houston, Bobbie Gentry, Cutis The Brothers, Sister Love, among others.
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Adams-Oliver syndrome is often mislabeled as CRS and consists of cutis aplasia of the scalp in which a longitudinal defect can vary in size and can often be associated with full-thickness skullcap loss.
40.
This condition is also known as Brauer syndrome ( hereditary symmetrical aplastic nevi of temples, bitemporal aplasia cutis congenita, bitemporal aplasia cutis congenita : OMIM ) and Setleis syndrome ( facial ectodermal dysplasia : OMIM ).
