Results 61 to 70 of about 3,257 (209)

Two male patients with incontinentia pigmenti [PDF]

, 2010
Background. Incontinentia pigmenti (IP) is a rare, complex, X-linked genodermatosis in which skin changes are combined with defects of other organs. It appears almost exclusively in females and is usually lethal in men.
Medenica Ljiljana, Minić Snežana, Novotny Gerd E.K., Obradović Miljana, Stefanović Bratislav, Trpinac Dušan   +5 more
core   +1 more source

Oligodontia Management in a Resource‐Limited Setting: Two Case Reports and Review of Literature

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Introduction: Oligodontia represents the developmental absence of six or more teeth, posing significant challenges for masticatory function, speech, and psychosocial well‐being. While extensively documented in developed countries, limited reports exist from resource‐constrained settings in Africa.
A. B. Malami, B. E. Ogbozor, C. C. Okolo, A. O. Aborisade, U. B. Mahmud, A. A. Abulfathi, Y. I. Adeyemo, Hannah Wesley   +7 more
wiley   +1 more source

Parameter Populasi Kerang Lumpur Tropis Anodontia Edentula Di Ekosistem Mangrove [PDF]

, 2009
Population Parameters of Tropical Mudflat Clam, (Anodontia edentula) in MangroveEcosystem. Over a 12 months period (Januari 2005 – Desember 2005), population parameters oftropical mudflat clam, (Anodonta edentula) in mangrove ecosystem were determined ...
Natan, Y. (Yuliana)
core  

Retardo en la erupción dental en adolescentes con hipotiroidismo [PDF]

, 2012
OBJECTIVE: To report the case of an adolescent with undiagnosed hypothyroidism who sought dental clinic care due to delayed tooth eruption. Multiprofessionalwork enabled the diagnosis.
Braga, Josefina Aparecida Pellegrini, Niskier, Sheila Rejane, Vitalle, Maria Sylvia de Souza, Weiler, Rosa Maria E.   +3 more
core   +4 more sources

Case Report of a Novel EVC Gene Mutation in Ellis–van Creveld Syndrome: Implications for Pediatric Dental Management

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Introduction Ellis–van Creveld (EVC) syndrome, also known as chondroectodermal dysplasia, is a rare autosomal recessive disorder that affects multiple embryonic tissues. It is primarily caused by mutations in the EVC gene. Patient Information We report an 11‐year‐old male diagnosed with EVC syndrome, who carries a novel homozygous pathogenic mutation ...
Mahnegar Shariati, Sara Tavassoli-Hojjati, Amirahmad Pahlavan Hoseini, Hanieh Jadidi, Hannah Wesley   +4 more
wiley   +1 more source

Bilateral Anterior Shoulder Dislocation [PDF]

, 2014
Introduction: Unilateral anterior shoulder dislocation is one of the most common problems encountered in orthopedic practice. However, simultaneous bilateral anterior dislocation of the shoulders is quite rare. Case Presentation: We report a case of a
Lui, T. H., Siu, Y. C.
core   +1 more source

Perkembangan Gonad Dan Musim Pemijahan Kerang Sepetang (Pharella Acutidens) Di Ekosistem Mangrove Dumai, Riau [PDF]

, 2012
This research aims to study the gonadal development and spawning seasonof “sepetang” clam (Pharella acutidens).The study was carried out over 12 month period from November 2010 to October 2011 at Dumai mangrove ecosystem.“Sepetang” clam samples were ...
Affandi, R. (Ridwan), Bengen, D. G. (Dietriech), Efriyeldi, E. (Efriyeldi)   +2 more
core  

Conservative interdisciplinary management for a congenitally missing maxillary lateral incisor in an adolescent patient

Australian Dental Journal, Volume 69, Issue 4, Page 267-277, December 2024.
Abstract A congenitally missing lateral incisor tooth is commonly associated with both short and long‐term clinical dilemmas, particularly for a growing patient. A unilaterally missing maxillary lateral incisor tooth creates a significant dental asymmetry in the critical aesthetic zone of the smile and potentially increases the difficulty of any ...
R Hmud, DC‐V Ong
wiley   +1 more source

The Incidence of the Tooth Agenesis in Students of Dentistry at Palacký University in Olomouc

Česká Stomatologie a Praktické Zubní Lékařství, 2015
Aim of the study: Tooth agenesis is very often developmental anomaly. The prevalence of this disorder differs depending on several factors. Different results can be observed in populations on different continents, in different races and genders, and in ...
L. Kramerová, P. Krejčí, K. Langová, A. Ševecová   +3 more
doaj   +1 more source

Whole genome sequencing in families with oligodontia

Oral Diseases, Volume 30, Issue 6, Page 3935-3950, September 2024.
Abstract Background/Objectives Tooth agenesis (TA) is among the most common malformations in humans. Although several causative mutations have been described, the genetic cause often remains elusive. Here, we test whether whole genome sequencing (WGS) could bridge this diagnostic gap.
Janna Mitscherling, Henrike L. Sczakiel, Olga Kiskemper‐Nestorjuk, Sibylle Winterhalter, Stefan Mundlos, Theodosia Bartzela, Martin A. Mensah   +6 more
wiley   +1 more source