Results 31 to 40 of about 66,379 (259)

CONGENITAL ACEPHALIA AND APROSOPIA MONSTER OF A DELIVERED FEMALE LAMB (WALRUS HEAD LAMB) [PDF]

open access: yesAssiut Veterinary Medical Journal, 1993
In the present report, the clinical, radiological and necropsy findings of a rare ovine moster were described. These examinations revealed that the congenital abnormalities were localized on the head region (walrus like head).
M.A. ALI, A.S. SALEH, S.H. SHEHAT
doaj   +1 more source

A Case of Trisomy 9 Mosaicism Confirmed by Microarray Test [PDF]

open access: yesKosin Medical Journal, 2020
Trisomy 9 mosaicism syndrome is a rare chromosomal abnormality with a high incidence of natural abortion and perinatal death. This syndrome is characterized by intrauterine growth retardation, mental retardation, craniofacial dysmorphism including a ...
Park Chang-Eon   +3 more
doaj   +1 more source

Burning Mouth Syndrome pada wanita Menopause dengan Hiposalivasi, Coated Tongue dan Gangguan Pengecapan serta Penatalaksanaannya

open access: yesMajalah Kedokteran Gigi Indonesia, 2012
Blackground: Burning mouth syndrome (BMS) is a disorder that is characterized by a burning sensation of the oral cavity in the absence of visible local or systemic abnormalities.
Sri Hadiati
doaj   +1 more source

Patients' mouth opening as a factor for discomfort during maxillary buccal infiltration anesthesia: A randomized clinical trial and survey of opinion

open access: yesSaudi Endodontic Journal, 2022
Introduction: The aim of the study was to investigate (a) whether patients' mouth opening influenced their discomfort during maxillary buccal infiltration (MBI) anesthesia and (b) whether dentists preferred their patients' mouth opened during MBI or ...
Ahmad M El-Ma'aita   +4 more
doaj   +1 more source

Sustained Therapeutic Efficacy of Intravenous Plasminogen Concentrate in Pediatric Patients With Type 1 Plasminogen Deficiency: An Analysis of Dosing Parameters and Clinical Outcomes

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Type 1 plasminogen deficiency (PLGD‐1) is an ultra‐rare autosomal recessive disorder caused by variants in the PLG gene and affects approximately 1.6 individuals per million. The condition is characterized by decreased plasminogen levels and impaired function, resulting in fibrin‐rich lesions on mucous membranes throughout the body.
Charles Nakar   +7 more
wiley   +1 more source

Health Literacy, Self‐Efficacy and Knowledge of Sickle Cell Disease Among Caregivers

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Sickle cell disease (SCD) is a hereditary blood disorder in which abnormal haemoglobin leads to severe anaemia, painful crises and organ failure. Caregivers’ health literacy (HL) – their ability to assess, understand and apply information, and interact with healthcare professionals – is crucial for managing children with SCD, yet ...
Melanie Bruinooge   +6 more
wiley   +1 more source

Frequency, distribution, and risk factors of oral mucosal lesions in a Colombian population: cross-sectional study

open access: yesRevista Facultad de Odontología Universidad de Antioquia
Introduction: oral mucosa lesions (OML) are any abnormal variations in appearance, color, texture, swelling, or loss of integrity of the oral mucosa. The worldwide prevalence varies from 4.9 % to 64.7 %.
Maricela Toro-Alzate   +5 more
doaj   +1 more source

Incidence and Severity of Carboplatin‐Associated Hearing Loss in Children With Cancer Assessed by the SIOP Boston 2012 Ototoxicity Criteria

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Platinum‐based chemotherapy is known to cause severe and debilitating hearing loss, but unlike cisplatin, the true incidence of carboplatin‐induced hearing loss remains unclear. We evaluated functional hearing outcomes in children receiving carboplatin to determine the incidence and severity of ototoxicity. Procedure We identified a
Aniket Chawla   +6 more
wiley   +1 more source

"Out of the ordinary": A case report of osteoma of mandibular condyle

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2015
Osteomas are relatively rare in the jaws. The causes of these lesions are unknown, although trauma, infection, and developmental abnormalities have been suggested as contributing factors.
Vaishali Mysore Rajshekar   +3 more
doaj   +1 more source

T2* Magnetic Resonance Imaging Uncovers Hemosiderin Burden in Pediatric Hemophilia: A Call for Sensitive Imaging Biomarkers

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Hemophilic arthropathy remains the leading morbidity in hemophilia despite modern prophylaxis, and early joint damage may be missed by routine exams. This study explored T2* MRI as a noninvasive biomarker of hemosiderin deposition in pediatric hemophilia.
Jessica Garcia   +6 more
wiley   +1 more source

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