- multiple lentigines syndrome
- LEOPARD s.
Medical dictionary. 2011.
multiple lentigines syndrome
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Syndrome LEOPARD — Pour les articles homonymes, voir Léopard (homonymie). Syndrome LEOPARD Référence MIM 151100 Transmission Dominante Chromosome … Wikipédia en Français
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Leopard syndrome — Infobox Disease Name = LEOPARD syndrome Caption = DiseasesDB = 7387 ICD10 = ICD9 = ICDO = OMIM = 151100 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 627 MeshName = LEOPARD+Syndrome MeshNumber = C05.660.207.525 LEOPARD syndrome is a rare… … Wikipedia
LEOPARD syndrome — Classification and external resources Three quarter facial view, first generation patient showing slight prognathism and low set ears. OMIM 151100 … Wikipedia
LEOPARD syndrome — an autosomal dominant syndrome consisting of multiple lentigines, asymptomatic electrocardiographic abnormalities, and often ocular hypertelorism, pulmonary stenosis, abnormal genitalia, growth retardation, and sensorineural deafness. Patients… … Medical dictionary
Moynahan syndrome — is a cutaneous condition characterized by multiple lentigines, congenital mitral stenosis, dwarfism, genital hypoplasia, and mental deficiency.[1]:686 It was characterized in 1962.[2][3] It is one of three conditions named for Edmund John… … Wikipedia
Moynahan syndrome — 1. multiple symmetric lentigines, congenital mitral valve stenosis, dwarfism, genital hypoplasia, and mental retardation. Called also progressive cardiomyopathic lentiginosis. 2. a familial congenital syndrome consisting of delayed hair growth on … Medical dictionary
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
lentiginosis — Presence of lentigines in very large numbers or in a distinctive configuration. centrofacial l. [MIM*151000 & MIM*151001] uncommon autosomal dominant syndrome of small hyperpigmented macules in a horizontal band across the center of the face at… … Medical dictionary
PTPN7 — Protein tyrosine phosphatase, non receptor type 7, also known as PTPN7, is a human gene.cite web | title = Entrez Gene: PTPN7 protein tyrosine phosphatase, non receptor type 7| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
