Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Anonychia congenita"'
Publikováno v:
Saudi Medical Journal, Vol 41, Iss 2, Pp 195-198 (2020)
Saudi Medical Journal
Saudi Medical Journal
Anonychia refers to the absence of nail plates owing to an autosomal dominant or recessive inheritance. Congenital anonychia is a rare condition that may be associated with other ectodermal or mesodermal malformations like epidermolysis bullosa, (dea
Publikováno v:
Journal of Advanced Research in Medicine. :20-22
Congenital anonychia in isolated form is a rare anomaly in which there is absence of nails of fingers and toes since birth. Other ectodermal and mesodermal defects in the body are absent. Here, we report a case of 16 year old male having rare congeni
Publikováno v:
Abstracts.
Background To describe the case of a new born baby with absent nails on fingers. Case report A term female baby was born to 27 years old G3P3 mother of Asian(Chinese)origin via spontaneous vaginal delivery with normal antenatal scans.During routine n
Autor:
Mrinal Gupta
Publikováno v:
Our Dermatology Online. 11:87-87
Publikováno v:
Research Journal of Pharmacology and Pharmacodynamics. 12:55
Autor:
Pardeep Kaurah, Ahmad S. Teebi
Publikováno v:
American Journal of Medical Genetics. 66:257-260
We report on 3 sibs (2 boys and a girl) with a previously apparently unrecognized combination of anonychia congenita and microcephaly with normal intelligence. The shape of the head is normal. Other anomalies include clinodactyly of the fifth fingers
Publikováno v:
International Journal of Dermatology. 41:397-399
A 27-year-old man presented with a history of the absence of the nails of all the fingers and toes since birth. His parents were first-degree cousins and there was no other case in the family. The past medical history was unremarkable. Examination re
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Autor:
Lucia Rosaia, Manuela Priolo, Margherita Silengo, Margherita Lerone, Marco Seri, Roberto Ravazzolo
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18021d79a3e3bdb8ee89d77909f47a16
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033966725&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033966725&partnerID=MN8TOARS