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Page 1
Hydrocephalus in children.
Rizvi R, Anjum Q. Rizvi R, et al. J Pak Med Assoc. 2005 Nov;55(11):502-7. J Pak Med Assoc. 2005. PMID: 16304873 Review.
The clinical features are increase in the size of head, with wide anterior fontanelle, prominent scalp veins, sun-setting eyes, optic nerve atrophy, nystagmus and increased muscle tone in children upto 2 years. ...
The clinical features are increase in the size of head, with wide anterior fontanelle, prominent scalp veins, sun-setti …
Forehead anatomy: arterial variations and venous link of the midline forehead flap.
Kleintjes WG. Kleintjes WG. J Plast Reconstr Aesthet Surg. 2007;60(6):593-606. doi: 10.1016/j.bjps.2006.12.006. Epub 2007 Feb 6. J Plast Reconstr Aesthet Surg. 2007. PMID: 17485046 Review.
The frontal branch of the superficial temporal artery (FBSTA) was found to continue in the direction of the scalp at the lateral orbital rim vertical line and gave off a transverse branch, the transverse frontal artery (TFA), to supply the forehead. ...The central artery, …
The frontal branch of the superficial temporal artery (FBSTA) was found to continue in the direction of the scalp at the lateral orbi …
Hutchinson-Gilford progeria syndrome caused by an LMNA mutation: a case report.
Chu Y, Xu ZG, Xu Z, Ma L. Chu Y, et al. Pediatr Dermatol. 2015 Mar-Apr;32(2):271-5. doi: 10.1111/pde.12406. Epub 2014 Dec 29. Pediatr Dermatol. 2015. PMID: 25556323 Review.
We report a 6-year-old boy who was born at full term but presented with scleroderma-like appearance at 1 month of age and gradually developed clinical manifestations of progeria. He had characteristic facial features of prominent eyes, scalp, and leg veins; l …
We report a 6-year-old boy who was born at full term but presented with scleroderma-like appearance at 1 month of age and gradually develope …
Clinical and laboratory findings of two newborns with Wiedemann-Rautenstrauch syndrome: additional features, evaluation of bone turnover and review of the literature.
Dinleyici EC, Tekin N, Dinleyici M, Aksit MA. Dinleyici EC, et al. J Pediatr Endocrinol Metab. 2008 Jun;21(6):591-6. J Pediatr Endocrinol Metab. 2008. PMID: 18717246 Review.
Our two patients had characteristic features of WRS, including intrauterine growth retardation, aged appearance, near absence of subcutaneous fat, gluteal fat pads, also labial pad in the first infant, wrinkled thin skin, sparse scalp hair, prominent scalp
Our two patients had characteristic features of WRS, including intrauterine growth retardation, aged appearance, near absence of subcutaneou …
Progeria infantum (Hutchinson-Gilford syndrome) associated with scleroderma-like lesions and acro-osteolysis: a case report and brief review of the literature.
Jansen T, Romiti R. Jansen T, et al. Pediatr Dermatol. 2000 Jul-Aug;17(4):282-5. doi: 10.1046/j.1525-1470.2000.01775.x. Pediatr Dermatol. 2000. PMID: 10990576 Review.
Progeria infantum (Hutchinson-Gilford syndrome) is a very rare syndrome of premature aging characterized by growth retardation and specific, progressive, premature senescent changes of the skin and other tissues. We report a 1.5-year-old girl with loss of scalp hair, eyebr …
Progeria infantum (Hutchinson-Gilford syndrome) is a very rare syndrome of premature aging characterized by growth retardation and specific, …
Wiedemann-Rautenstrauch syndrome. A case report and review of the literature.
Stoll C, Labay F, Geisert J, Alembik Y. Stoll C, et al. Genet Couns. 1998;9(2):119-24. Genet Couns. 1998. PMID: 9664208 Review.
During infancy a progeroid appearance was noted with sparse hair, prominent scalp veins, greatly widened anterior fontanelles, malar hypoplasia, and generalized lipoatrophy. ...
During infancy a progeroid appearance was noted with sparse hair, prominent scalp veins, greatly widened anterior fonta …
A probable case of Wiedemann-Rautenstrauch syndrome or neonatal progeroid syndrome and review of the literature.
Courtens W, Nuytinck L, Fricx C, André J, Vamos E. Courtens W, et al. Clin Dysmorphol. 1997 Jul;6(3):219-27. doi: 10.1097/00019605-199707000-00004. Clin Dysmorphol. 1997. PMID: 9220191 Review.
Abnormal findings included a generalized virtual absence of subcutaneous fat, sparse scalp hair, prominence of veins and muscles, a large and persistent anterior fontanelle and facial dysmorphism (triangular aged face, prominent eyes and scalp
Abnormal findings included a generalized virtual absence of subcutaneous fat, sparse scalp hair, prominence of veins an …
[Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature].
Huang S, Liang Y, Wu W, Fu X, Liao L, Luo X. Huang S, et al. Zhonghua Er Ke Za Zhi. 2014 Feb;52(2):112-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 24739722 Review. Chinese.
RESULT: At the age of 8 months, the affected-infant presented with characteristic manifestation such as short stature, low weight, frontal bossing, alopecia, prominent scalp veins, micrognathia with a vertical midline groove in the chin, sclerodermatous skin, …
RESULT: At the age of 8 months, the affected-infant presented with characteristic manifestation such as short stature, low weight, frontal b …
[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch). A follow-up study].
Rautenstrauch T, Snigula F, Wiedemann HR. Rautenstrauch T, et al. Klin Padiatr. 1994 Nov-Dec;206(6):440-3. doi: 10.1055/s-2008-1046647. Klin Padiatr. 1994. PMID: 7823529 Review. German.
The diagnostic criteria of the neonatal progeroid syndrome (NPS) are: intrauterine and postnatal growth failure, hydrocephalic appearance, prominent scalp veins, old-looking face, absence of subcutaneous fat and neonatal teeth. ...
The diagnostic criteria of the neonatal progeroid syndrome (NPS) are: intrauterine and postnatal growth failure, hydrocephalic appearance, …