scholarly journals Oral Rehabilitation of a Patient with Congenital Erythropoietic Porphyria: A Rare Case Report Porphyria: A Rare Case Report

2020 ◽  
Vol 27 (2) ◽  
Author(s):  
Raif Alan ◽  
◽  
Hakkı Çelebi ◽  
Fahriye Kilinc ◽  
Recep Dursun ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unmet Need ◽  
Missing Teeth ◽  
Oral Rehabilitation ◽  
Gingival Bleeding ◽  
Congenital Erythropoietic Porphyria ◽  
Rare Case Report ◽  
Skin Fragility ◽  
Phase I And Ii

Congenital erythropoietic porphyria (CEP) is an extremely rare disorder involved in chronic porphyrias. One of the recommended evaluations to determine disease severity and needs of a person with CEP is dental assessment. Objective: To present a case of CEP and its oral rehabilitation. Case Report: A 32-year-old female patient was admitted to the clinic with hyperkeratinization, skin fragility, fissures, and wounds in her perioral region and hands. Intraoral gingival bleeding, mucogingival stress, and missing teeth were recorded. After medical consultation, phase I and II periodontal therapies were performed. The patient expressed satisfaction of the results of the procedures in terms of the parameters evaluated. The rare occurrence of the disease may delay the diagnosis. An unmet need still exists for multidisciplinary orientation of patients with CEP. Conclusion: Dentists should have and follow guidelines for treating patients with CEP.

scholarly journals Complete oral rehabilitation in a child with classical cornelia de lange syndrome: A rare case report

2012 ◽  
Vol 1 (4) ◽  
pp. 268
Author(s):  
Radhika Muppa ◽  
NarendraVarma Penumatsa ◽  
MaheshKumar Duddu ◽  
Dhanalakshmi Karre
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cornelia De Lange Syndrome ◽  
Oral Rehabilitation ◽  
Rare Case Report ◽  
Cornelia De Lange

scholarly journals Bilateral Hypodontia of Mandibular Second Premolars and Lateral Incisors in a Nonsyndromic Patient: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 24-26
Author(s):  
Shakun Kanjani
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Permanent Teeth ◽  
Rare Occurrence ◽  
Third Molars ◽  
Missing Teeth ◽  
Dental Anomaly ◽  
Mahatma Gandhi ◽  
The Third ◽  
Rare Case Report

ABSTRACT Hypodontia is the term used to describe the developmental absence of one or more primary or permanent teeth, excluding the third molars. It is the most commonly occurring developmental dental anomaly and can be a challenge to manage clinically. Hypodontia can occur in association with syndrome or it may occur in nonsyndromic patient. Bilateral occurrence is common but it is very rare to see two bilateral congenital missing teeth in a nonsyndromic patient. This case report presents a rare occurrence of congenital bilateral missing mandibular second premolars and mandibular lateral incisors in a nonsyndromic patient. How to cite this article Agarwal N, Chaturvedy S, Marwah N, Mishra P, Kanjani S. Bilateral Hypodontia of Mandibular Second Premolars and Lateral Incisors in a Nonsyndromic Patient: A Rare Case Report. J Mahatma Gandhi Univ Med Sci Tech 2016;1(1):24-26.

scholarly journals Ectodermal dysplasia-skin fragility syndrome: A rare case report

2015 ◽  
Vol 60 (4) ◽  
pp. 421 ◽  
Author(s):  
Subhash Kashyap ◽  
Vinay Shanker ◽  
Neelam Sharma
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ectodermal Dysplasia ◽  
Rare Case Report ◽  
Skin Fragility

scholarly journals Nonsyndromic Oligodontia: A Rare Case Report with Review of Literature

2014 ◽  
Vol 02 (02) ◽  
pp. 109-112
Author(s):  
Puneet Bajaj ◽  
Robin Sabharwal ◽  
Sonia Joshi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ectodermal Dysplasia ◽  
Developmental Anomaly ◽  
Permanent Teeth ◽  
Review Of Literature ◽  
Third Molars ◽  
Missing Teeth ◽  
Rare Case Report ◽  
Oral Abnormalities

AbstractDental agenesis is the most common developmental anomaly in humans and is frequently associated with several other oral abnormalities. In the literature, some terms are used to describe missing teeth like Oligodontia, Anodontia and Hypodontia. Oligodontia is defined as the developmental absence of six teeth or more, excluding third molars. It can be isolated or as a part of a syndrome such as in ectodermal dysplasia. The present case describes agenesis of permanent teeth which are non-familial and with no apparent systemic abnormalities

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report
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