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pigmentary
pigmentary, n. and a. (ˈpɪgməntərɪ) Also 4 pymentarie, -ye, 5 pygmentarie. [ad. L. pigmentāri-us adj., of or belonging to paints or unguents; n. a dealer in these, in med.L. esp. in scents, spices, and aromatic confections, f. pigment-um: see pigment n. and -ary1.] † A. n. a. A maker or seller of oi...
Oxford English Dictionary
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X-linked reticulate pigmentary disorder
X-linked reticulate pigmentary disorder is a rare X-linked genetic condition in which males manifest multiple systemic symptoms and a reticulated mottled
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pigmental
pigmental, a. (pɪgˈmɛntəl) [f. L. pigmentum (see pigment n.) + -al1.] = pigmentary a. 2. Hence pigˈmentally adv.1842 Prichard Nat. Hist. Man (ed. 2) 83 The mucous or pigmental membrane. 1886 Belgravia Mag. LIX. 353 Over⁓coloured, pigmentally and orally. 1896 Allbutt's Syst. Med. I. 114 Atrophy and p...
Oxford English Dictionary
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Pigmented purpuric dermatosis
Pigmentary purpuric eruptions may present with one of several clinical patterns.
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Terminal osseous dysplasia with pigmentary defects
Terminal osseous dysplasia with pigmentary defects is a cutaneous condition characterized by hyperpigmented, atrophic facial macules.
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pyn
pymander, pymentarie, -ye, pyn obs. ff. pomander, pigmentary, pin, pine.
Oxford English Dictionary
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Doucas and Kapetanakis pigmented purpura
See also
Pigmentary purpuric eruptions
List of cutaneous conditions
References
External links
Vascular-related cutaneous conditions
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Reticular pigmented anomaly of the flexures
It is an autosomal-dominant pigmentary disorder that may appear in adolescence or adulthood.
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Secondary glaucoma
Other forms of secondary glaucoma
Pigmentary glaucoma: In pigmentary glaucoma, the obstruction of the trabecular meshwork caused by iris pigment release Thus, it is also commonly used in the treatment of pigmentary glaucoma.
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Pigment dispersion syndrome
Pigment dispersion syndrome (PDS) is an eye disorder that can lead to a form of glaucoma known as pigmentary glaucoma. When the pressure is great enough to cause damage to the optic nerve, this is called pigmentary glaucoma.
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Linear and whorled nevoid hypermelanosis
It is important to exclude other pigmentary disorders following the Blaschko lines before making a diagnosis of linear and whorled nevoid hypermelanosis
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BBS2
Bardet–Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and
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Erythromelanosis follicularis faciei et colli
Erythromelanosis follicularis faciei et colli is an erythematous pigmentary disease involving the follicles, characterized by a reddish-brown, sharply
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Corneodermatoosseous syndrome
See also
Palmoplantar keratoderma
Keratoderma
Skin lesion
Terminal osseous dysplasia with pigmentary defects
List of cutaneous conditions
References
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BBS4
The encoded protein may play a role in pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation.
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