Results 71 to 80 of about 6,989 (157)

Cutis verticis gyrata of the scalp in a patient with autosomal dominant insulin resistance syndrome

, 2000
Cutis verticis gyrata (CVG) is a rare disorder; it is characterized by thickening of the scalp which becomes raised to form ridges and furrows resembling the cerebral gyri. We report a case of CVG associated with the autosomal dominant insulin resistance
Darley, C R, Brenton, D P, Woollons, A, Lee, P J, Sonksen, P H, Black, M M   +5 more
core   +1 more source

A case of cutis verticis gyrata associated with epilepsy

, 2016
Cutis vertices gyrata (CVG) is characterized by thickening of the scalp, which becomes raised to form ridges and furrows resembling cerebral gyri that cannot be flattened by traction or pressure.
Mohammad Abid Keen, Iffat Hassan
core   +1 more source

Acromegaly and Cutis Verticis Gyrata [PDF]

Journal of the Royal Society of Medicine, 1997
F M, O'Reilly, I, Sliney, S, O'Loughlin
openaire   +2 more sources

Cutis Verticis Gyrata: A propósito de un caso.

, 2016
Cutis verticis gyrata (CVG) es una condición que se manifiesta con pliegues y surcos formados a partir de piel engrosada en el cuero cabelludo, adquiriendo patrón cerebriforme.
Goncalves, María Isabel, Correa, Lilia, López, Miguel Alejandro, Jaramillo, Sandra, Zamora, Mariela, Franco, Francisco   +5 more
core   +1 more source

AN ENDOCRINOLOGIC STUDY OF PATIENTS WITH PRIMARY-CUTIS-VERTICIS GYRATA

, 1993
An endocrinological study of 15 psychiatric patients with primary cutis verticis gyrata (CVG) and 7 control patients was carried out. The investigation of the pituitary-gonadal axis, pituitary-adrenal axis, pituitary-thyroid axis, prolactin and human ...
RUGGERI M, BALDINI L, SPINA, Edoardo, SCHEPIS C, PALAZZO R, PIZZIMENTI A, ARCORACI, Vincenzo   +6 more
core  

Cutis Verticis Gyrata [PDF]

Proceedings of the Royal Society of Medicine, 1932
openaire   +2 more sources

Pemphigus Vegetans masquerading as Cutis Verticis Gyrata

, 2013
Pemphigus vegetans a variant of pemphigus vulgaris divided  into  Neumann  type,  which  begins  and  ends  as  Pemphigus  vulgaris,  and Hallopeau  type,  which  is  relatively  benign,  having  pustules  as primary  lesions  instead of  bullae ...
Gupta, Nishant; Govt. Stanley medical college hospital, Aravamudhan, Ramesh; Govt. Stanley medical college hospital, Rajendrabose, Ratnavel; Govt. Stanley medical college hospital, b k, aarthi; Govt. Stanley medical college hospital, Nanjunda Gowda, Rajesh Huthur; Govt. Stanley medical college hospital   +4 more
core   +3 more sources

Primary Hypertrophic Osteoarthropathy: A Case Report

Case Reports in Clinical Practice, 2018
The primary hypertrophic osteoarthropathy (PHOA or pachydermoperiostosis) is a rare (5% of total HOA) hereditary disease. One study described that the prevalence of PHOA is 0.16%.
Shima Asadi-Komeleh, Abdolrahman Rostamian, Fatemeh Shahbazi, Shafieh Movassagi, Parviz Soofivand   +4 more
doaj  

Congenital Cutis Verticis Gyrata in a Newborn with Turner Syndrome: A Rare Clinical Manifestation of This Chromosomal Disease with Trichoscopic Evaluation. [PDF]

Diagnostics (Basel), 2023
Bortone R, Bonamonte D, Cazzato G, Laface C, Gaeta A, Lettini T, Foti C, Filotico R, Ambrogio F.   +8 more
europepmc   +1 more source

Cutis Verticis Gyrata (Congenital) [PDF]

Proceedings of the Royal Society of Medicine, 1938
openaire   +4 more sources