Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
2001 1
2004 1
2016 1
2017 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

5 results

Results by year

Filters applied: . Clear all
Page 1
Foramina parietalia permagna: familial and radiological evaluation of two cases and review of literature.
Gabor L, Canaz H, Canaz G, Kara N, Gulec EY, Alatas I. Gabor L, et al. Childs Nerv Syst. 2017 May;33(5):853-857. doi: 10.1007/s00381-016-3315-8. Epub 2016 Dec 14. Childs Nerv Syst. 2017. PMID: 27975139 Review.
Foramina parietalia permagna have an autosomal dominant inheritance, and it is showed that mutations in chromosome 5 and 11 are causing this anomaly. Enlarged parietal foramina occurs extremely rare. They are usually asymptomatic, but occasional headache, vomiting, …
Foramina parietalia permagna have an autosomal dominant inheritance, and it is showed that mutations in chromosome 5 and 11 are causing this …
Craniosynostosis and related limb anomalies.
Wilkie AO, Oldridge M, Tang Z, Maxson RE Jr. Wilkie AO, et al. Novartis Found Symp. 2001;232:122-33; discussion 133-43. doi: 10.1002/0470846658.ch9. Novartis Found Symp. 2001. PMID: 11277076 Review.
We have recently identified three MSX2 mutations associated with a different cranial phenotype, parietal foramina. DNA binding studies show that the craniosynostosis and parietal foramina arise from gain and loss of function, respectively....
We have recently identified three MSX2 mutations associated with a different cranial phenotype, parietal foramina. DNA binding …
Bilateral Foramina Parietalia Permagna - A Calvarial Defect Caused by Haploinsufficiency of the Msh Homeobox 2 Gene: A Case Report and Current Literature Review.
Kahl N, Lüsebrink N, Schubert-Bast S, Freiman TM, Kieslich M. Kahl N, et al. Neuropediatrics. 2024 Jun;55(3):205-208. doi: 10.1055/s-0044-1781465. Epub 2024 Mar 6. Neuropediatrics. 2024. PMID: 38447947 Free article. Review.
FPP is an inherited disorder and arises due to mutations in either Msh homeobox 2 (MSX2) or aristaless-like homeobox 4 (ALX4) genes. In almost all cases, one parent is affected. ...
FPP is an inherited disorder and arises due to mutations in either Msh homeobox 2 (MSX2) or aristaless-like homeobox 4 (ALX4) genes. …
Radiographic manifestations of congenital anomalies of the skull.
Kaplan SB, Kemp SS, Oh KS. Kaplan SB, et al. Radiol Clin North Am. 1991 Mar;29(2):195-218. Radiol Clin North Am. 1991. PMID: 1998047 Review.
For the purposes of this discussion, these entities can be classified according to the radiographic appearance of the skull, which may be similar in a variety of different diseases. Enlarged parietal foramina, sinus pericranii, aplasia cutis congenita, anterior font …
For the purposes of this discussion, these entities can be classified according to the radiographic appearance of the skull, which may be si …
Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects.
Wuyts W, Waeber G, Meinecke P, Schüler H, Goecke TO, Van Hul W, Bartsch O. Wuyts W, et al. Eur J Hum Genet. 2004 May;12(5):400-6. doi: 10.1038/sj.ejhg.5201163. Eur J Hum Genet. 2004. PMID: 14872200 Review.
The combination of multiple exostoses (EXT) and enlarged parietal foramina (foramina parietalia permagna, FPP) represent the main features of the proximal 11p deletion syndrome (P11pDS), a contiguous gene syndrome (MIM 601224) caused by an interstitial deletion on t …
The combination of multiple exostoses (EXT) and enlarged parietal foramina (foramina parietalia permagna, FPP) represent the m …