A rare case of osteogenesis imperfecta combined with complete tooth loss

2014 ◽  
Vol 27 (1-2) ◽  
Author(s):  
Yanqin Lu ◽  
Fei Zhao ◽  
Xiuzhi Ren ◽  
Zhiliang Li ◽  
Xiaomeng Yang ◽  
...  
Keyword(s):  
Osteogenesis Imperfecta ◽  
Rare Case ◽  
Tooth Loss

scholarly journals A rare case of osteogenesis imperfecta (OI): clinical image

2022 ◽  
Vol 41 ◽  
Author(s):  
Prasad Pramod Dhage ◽  
Chaitanya Ajay Kulkarni
Keyword(s):  
Osteogenesis Imperfecta ◽  
Rare Case ◽  
Clinical Image

Osteogenesis imperfecta – a rare case report

2018 ◽  
Vol 67 ◽  
pp. S8-S9
Author(s):  
S.R. Das ◽  
G. Nayak ◽  
S. Nayak
Keyword(s):  
Case Report ◽  
Osteogenesis Imperfecta ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Osteogenesis Imperfecta: An Uncommon Association with Non-Communicating Hydrocephalus

2013 ◽  
Vol 33 (1) ◽  
pp. 63-65
Author(s):  
K Chatterjee ◽  
S Dolui ◽  
S Das ◽  
A Paul
Keyword(s):  
Connective Tissue ◽  
Osteogenesis Imperfecta ◽  
Patent Foramen Ovale ◽  
Rare Case ◽  
Communicating Hydrocephalus ◽  
Foramen Ovale ◽  
Blue Sclera ◽  
Noncommunicating Hydrocephalus ◽  
Type 3

Osteogenesis imperfecta (OI) is a generalised disorder of connective tissue presenting with fragile bones, blue sclera and early deafness. Hydrocephalus is usually associated with type 2 OI. Here we present a rare case of noncommunicating hydrocephalus and patent foramen ovale in type 3 OI. DOI: http://dx.doi.org/10.3126/jnps.v33i1.6692 J Nepal Paediatr Soc. 2013;33(1):63-65

A RARE CASE OF OSTEOGENESIS IMPERFECTA TYPE I

2021 ◽  
pp. 53-54
Author(s):  
P.C. Prince ◽  
Sunil Malhotra ◽  
Mahendra Meena ◽  
Sandeep Singh
Keyword(s):  
Osteogenesis Imperfecta ◽  
Rare Case ◽  
Lower Limbs ◽  
Type I ◽  
Osteogenesis Imperfecta Type ◽  
Mineral Density ◽  
The Past ◽  
Blue Sclera ◽  
Osteogenesis Imperfecta Type I

A 7 year old female patient was admitted to hospital having experienced bowing of upper and lower limbs, repeated fractures over the past 4 years. Clinical ndings and radiological investigations such as recurrent fractures and deformity of bones while bearing weight, blue sclera and low bone mineral density, all led us to conclude that this child has a mild form of osteogenesis imperfecta type I. The patient was immediately started on calcium (1000mg/day), vitamin D (800mg/day) and pamidronate (60mg) was given intravenously. Following the above protocol, we found that the quality of life of the patient showed signicant improvement. This patient is a rare case of OI type I.

scholarly journals ANAESTHESIA MANAGEMENT OF A RARE CASE OSTEOGENESIS IMPERFECTA (OI)POSTED FOR OPEN APPENDECTOMY

2021 ◽  
Vol 10 (1) ◽  
pp. 1
Author(s):  
MAMATHA RACHALA ◽  
MURALI ATLURI ◽  
JAYANTH MEDITHALA ◽  
ANIL VALLURI ◽  
KRISHNA KANDHUKURI
Keyword(s):  
Osteogenesis Imperfecta ◽  
Rare Case ◽  
Open Appendectomy

scholarly journals Dental Care for an adolescent with chromosome pentasomy: rare case report with a two year follow-up

2015 ◽  
Vol 63 (4) ◽  
pp. 507-511
Author(s):  
Nayara Silva ALVES ◽  
Andréa Videira ASSAF ◽  
Ângela Maria MARTINS ◽  
Marlus Roberto Rodrigues CAJAZEIRA ◽  
Leonardo Santos ANTUNES ◽  
...  
Keyword(s):  
X Chromosome ◽  
Dental Care ◽  
Rare Case ◽  
Tooth Loss ◽  
Scientific Literature ◽  
Outpatient Basis ◽  
Therapeutic Success ◽  
Rare Case Report ◽  
Dental Work

Pentasomy of the x chromosome is a rare syndrome of unknown incidence and there are few reports in the scientific literature, especially in terms of dental care for patients with this syndrome. The aim of this study was to report the dental care given to an adolescent with pentasomy of the X chromosome. The patient presented a cleft palate, impacted teeth, malocclusion, high caries activity, gingivitis and multiple tooth loss due to caries. Despite the difficulties of carrying out the dental work due to involuntary movements and the initial lack of collaboration from the patient the overall dental care was completed on an outpatient basis. The therapeutic success of the treatment was strongly supported by the significant cooperation and relationship that grew up along the period of the treatment, as well as the desire to have the treatment done by both the patient and her parents.

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