Displaying publications 21 - 40 of 474 in total

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  1. MCGLADDERY HM
    Med J Malaya, 1960 Dec;15:65-9.
    PMID: 13773946
    Matched MeSH terms: Thorax/abnormalities*
  2. GORDON W
    Med J Malaya, 1958 Dec;13(2):173-4.
    PMID: 13632217
    Matched MeSH terms: Cardiovascular Abnormalities/surgery*
  3. Ahmed HM, Hashem AA
    Int Endod J, 2016 Aug;49(8):724-36.
    PMID: 26174943 DOI: 10.1111/iej.12508
    Anterior teeth may have aberrant anatomical variations in the number of roots and root canals. A review of the literature was conducted using appropriate key words in major endodontic journals to identify the available reported cases as well as experimental and clinical investigations on accessory roots and root canals in anterior teeth. After retrieving the full text of related articles, cross-citations were identified, and the pooled data were then discussed. Results revealed a higher prevalence in accessory root/root canal variations in mandibular anterior teeth than in maxillary counterparts. However, maxillary incisor teeth revealed the highest tendency for accessory root/root canal aberrations caused by anomalies such as dens invaginatus and palato-gingival groove. Primary anterior teeth may also exhibit external and internal anatomical variations in the root, especially maxillary canines. Therefore, dental practitioners should thoroughly assess all teeth scheduled for root canal treatment to prevent the undesirable consequences caused by inadequate debridement of accessory configurations of the root canal system.
    Matched MeSH terms: Cuspid/abnormalities; Dental Pulp Cavity/abnormalities*; Incisor/abnormalities; Tooth Root/abnormalities*
  4. Hamzah AR, Jalaluddin MA, Raman R
    Ann Otol Rhinol Laryngol, 1999 Mar;108(3):253-4.
    PMID: 10086617
    A patient with Turner's syndrome presented with a rare anomaly of absent oval window, inferiorly placed facial nerve, and abnormal stapes. To our knowledge, this is the first report of this combination of malformations.
    Matched MeSH terms: Ear, Middle/abnormalities*; Facial Nerve/abnormalities; Oval Window, Ear/abnormalities; Stapes/abnormalities
  5. Nayak SB, Shetty SD
    Surg Radiol Anat, 2021 Aug;43(8):1327-1330.
    PMID: 33527215 DOI: 10.1007/s00276-021-02682-0
    Sternohyoid, sternothyroid, omohyoid, and thyrohyoid muscles are collectively known as infrahyoid muscles. These muscles frequently show variations in their attachments. Here, an extremely rare variant muscle belonging to this group has been presented. During cadaveric dissection for undergraduate medical students, an additional muscle was found between sternohyoid and superior belly of omohyoid muscles bilaterally in a male cadaver aged approximately 70 years. This muscle took its origin from posterior surface of the manubrium sterni, capsule of the sternoclavicular joint and the posterior surface of the medial part of the clavicle. It was inserted to the hyoid bone between the attachments of sternohyoid and superior belly of omohyoid muscles and was supplied by a branch of ansa cervicalis profunda. There is no report on such a muscle in the literature and it could be named as "sternocleidohyoid muscle". Knowledge of this muscle could be useful in neck surgeries.
    Matched MeSH terms: Clavicle/abnormalities; Hyoid Bone/abnormalities; Neck Muscles/abnormalities*; Sternum/abnormalities
  6. Yaacob R, Zainal Mokhtar A, Abang Jamari DZH, Jaafar N
    BMJ Case Rep, 2017 Sep 23;2017.
    PMID: 28942402 DOI: 10.1136/bcr-2017-220801
    Fetus-in-fetu (FIF) is a rare entity in which malformed parasitic twin grows inside the body of its twin. It is most commonly presented with mass in the abdomen. We present a case of a 15-year-old boy who presented with abdominal mass since infancy. Radiological investigations are suggestive of FIF. Intraoperatively, malformed fetus in a sac was found and excised. Postoperatively the patient recovers well and was put on follow-up.
    Matched MeSH terms: Abdomen/abnormalities; Congenital Abnormalities/surgery; Fetus/abnormalities*
  7. Chaudhuri JD
    J Indian Med Assoc, 2002 Feb;100(2):107-8, 110.
    PMID: 12206352
    Foetal alcohol syndrome (FAS) is a collection of signs and symptoms seen in children of women who consume alcohol during pregnancy. With the increasing incidence of FAS, there is a great variation of its clinical features different from that described in the standard textbooks. This article aims to report on the unusual clinical features of FAS. It also aims to explain the mechanism of action of alcohol as a teratogenic agent.
    Matched MeSH terms: Abnormalities, Multiple/diagnosis*; Abnormalities, Multiple/etiology; Eye Abnormalities/diagnosis; Urinary Tract/abnormalities
  8. Arshad AR, Goh CS
    Br J Plast Surg, 1994 Mar;47(2):139-41.
    PMID: 8149059
    Two cases of hypoglossia congenita with anterior maxillo-mandibular fusion are reported. One is a case of hypoglossia with anterior maxillo-mandibular fusion and the other is a case of hypoglossia-hypodactylia with anterior maxillo-mandibular fusion. This condition presents the anaesthetist with the problem of airway management during the surgery. A simple technique using a nasopharyngeal tube was used for these two cases, with satisfactory results.
    Matched MeSH terms: Alveolar Process/abnormalities; Forearm/abnormalities; Mandible/abnormalities*; Maxilla/abnormalities*; Toes/abnormalities; Tongue/abnormalities*
  9. Hisham AN, Gunn A, Jamil AA
    Med J Malaysia, 1995 Sep;50(3):281-3.
    PMID: 8926911
    Matched MeSH terms: Abnormalities, Multiple/diagnosis*; Abnormalities, Multiple/radiography; Diaphragm/abnormalities*; Intestines/abnormalities*; Liver/abnormalities*
  10. Western JS, Gupta VV, Ramachandra SS
    Compend Contin Educ Dent, 2019 Mar;40(3):172-177.
    PMID: 30829499
    This case report describes the management of a mandibular first molar with an additional distolingual root (radix entomolaris) and grade III cervical enamel projection through a multidisciplinary approach. Diagnosis for the case was endodontic-periodontal lesion due to non-vitality and associated advanced periodontal destruction. The patient was treated with drainage of the periodontal abscess with adjunct antibiotics, phase I periodontal therapy, endodontic therapy, radiculoplasty, regenerative periodontal therapy, replacement of the missing right mandibular second molar, and long-term maintenance. Follow-up of the patient up to 9 months has been uneventful. Cases of advanced periodontal destruction typically show some degree of tooth mobility, which was absent in this case. The article discusses the tripod effect as well as the increased surface area for periodontal attachment provided by the additional root contributing to the non-mobility of the involved tooth.
    Matched MeSH terms: Dental Enamel/abnormalities*; Molar/abnormalities*; Tooth Abnormalities/complications; Tooth Abnormalities/ethnology; Tooth Abnormalities/therapy*
  11. Suhaili DN, Somasundaram S, Lau SH, Ajura AJ, Roslan AR, Ramli R
    Int J Pediatr Otorhinolaryngol, 2011 Jan;75(1):131-3.
    PMID: 21067822 DOI: 10.1016/j.ijporl.2010.10.004
    Diprosopus or duplication of the lower lip and mandible is a very rare congenital anomaly. We report this unusual case occurring in a girl who presented to our hospital at the age of 4 months. Surgery and problems related to this anomaly are discussed.
    Matched MeSH terms: Abnormalities, Multiple/diagnosis; Abnormalities, Multiple/surgery; Lip/abnormalities*; Mandible/abnormalities*; Craniofacial Abnormalities/diagnosis; Craniofacial Abnormalities/surgery*
  12. Lloyd S, Rashid AH, Das S, Ibrahim S
    Anat Sci Int, 2014 Mar;89(2):122-5.
    PMID: 24158808 DOI: 10.1007/s12565-013-0211-0
    Tibial hemimelia is a rare anomaly of unknown etiology. This condition can occur sporadically or may have a familial inheritance. It is characterized by deficiency of the tibia with a relatively intact fibula. The anomaly may be unilateral or bilateral. We report a case of a 2-year-old girl who presented with right lower limb deformity since birth. She was diagnosed with proximal femur focal deficiency with absence of the ipsilateral tibia. She presented with a shorter right lower limb and a deformed foot. She was treated with a through-knee amputation. Anatomical dissection of the amputated limb was carried out to verify the anomalies. The dissection showed that the distal phalanx of the great toe was trifid. The anatomical and clinical significance of this interesting case is discussed.
    Matched MeSH terms: Femur/abnormalities*; Tibia/abnormalities*
  13. Das S, Norzana AG, Azian AL, Farihah HS, Faizah O
    Clin Ter, 2011;162(6):555-7.
    PMID: 22262329
    In this case report, we report the absence of the fourth tendon of flexor digitorium superficialis (FDS) to the little finger with a concurrent anomalous muscular belly of flexor digitorum profundus (FDP) in the palm. The FDS originated from the medial epicondyle, divided into three tendons for the index, middle and ring fingers with the little finger devoid of any attachment. The FDP exhibited a muscular belly which passed deep to the flexor retinaculum (FR) and continued for another 4 cm thereby dividing into four slips for the index, middle, ring and little fingers. The presence of the muscular belly of the FDP lead us to think whether it was an adhesion between the tendons of the FDP, so we proceeded to histological analysis. The tissue was processed and stained with Hematoxylin and Eosin. Abundant longitudinal muscle fibers with peripherally situated nuclei confirmed it to be a skeletal muscle. Absence of the tendon of FDS to little finger may influence the flexion movement in the middle and proximal interphalangeal joints. Presence of anomalous muscle belly of FDP in the palm may mimic any soft tissue tumour, compress neurovascular structures or even pose difficulty while performing tendon transplant surgeries.
    Matched MeSH terms: Fingers/abnormalities*; Tendons/abnormalities*
  14. Das S, Chaudhuri JD
    Kathmandu Univ Med J (KUMJ), 2008 Apr-Jun;6(2):217-9.
    PMID: 18769090
    The articular facets on the inferior aspect of the occipital condyles, articulate with the superior articular facets of the first cervical (atlas) vertebra, to form the atlanto-occipital joint. The present case, reports the asymmetrical dimensions of the facets on the occipital condyles of a human dried skull. The anatomico-radiological study of asymmetrical articular facets on the occipital condyles, may be helpful for academicians, neuro-surgeons, clinicians and radiologists in day to day clinical practice.
    Matched MeSH terms: Atlanto-Occipital Joint/abnormalities; Occipital Bone/abnormalities*
  15. Peng GP, Chuan YT
    Med J Malaysia, 1988 Jun;43(2):138-49.
    PMID: 3266287
    Matched MeSH terms: Congenital Abnormalities/mortality; Congenital Abnormalities/epidemiology*
  16. Meon R
    Singapore Dent J, 1990 Dec;15(1):32-4.
    PMID: 2097727
    A case of talon cusp in the primary maxillary left central incisor is reported. This dental anomaly was not associated with any other somatic or dental abnormality. Though pulpal extension into the cusp was detected radiographically, clinical examination after the cusp was ground failed to reveal any pulpal extension. The tooth was badly carious and was restored with a polycarbonate crown.
    Matched MeSH terms: Incisor/abnormalities*; Tooth, Deciduous/abnormalities*
  17. Shanmuhasuntharam P, Thong YL
    Singapore Dent J, 1990 Dec;15(1):27-31.
    PMID: 2097726
    Transposition of teeth is a rare and special type of ectopic eruption where two contiguous teeth are found occupying each other's respective normal positions. Nine patients with transposed maxillary teeth are reported. The literature on transpositions, especially on the theories regarding the aetiology, is reviewed.
    Matched MeSH terms: Bicuspid/abnormalities; Cuspid/abnormalities
  18. Rushmah Meon
    J Clin Pediatr Dent, 1992;16(2):121-3.
    PMID: 1498047
    The prevalence, possible etiological factors and management of hypodontia was briefly reviewed. A report of a case of hypodontia affecting the primary and permanent lower incisors was described.
    Matched MeSH terms: Incisor/abnormalities*; Tooth, Deciduous/abnormalities*
  19. Choridah L, Pangastuti N
    Med J Malaysia, 2024 Aug;79(Suppl 4):83-86.
    PMID: 39215421
    Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) is a rare congenital malformation of the female urogenital tract characterized by a triad of uterine didelphys, obstructed hemivagina, and ipsilateral renal anomaly. It was formerly known as Herlyn Werner Wunderlich Syndrome (HWWS). The syndrome usually presents with cyclic pelvic pain following menarche. Endometriosis is a prevalent complication. Magnetic resonance imaging (MRI) helps in diagnosing OHVIRA syndrome and endometriosis due to its high contrast resolution and objectivity. We reported a 13- year-old girl who was evaluated for cyclic pelvic pain after her menarche at 12 years of age. Magnetic resonance imaging (MRI) revealed two separate uterine cavities, services and vaginae, indicating didelphys. The left uterine cavity is filled with fluid, and the left hemivagina is dilated and filled with hyperintense and hypointense fluid on T1 and T2, respectively, indicating blood products. Left hemivagina dilatation implicated the presence of an obstructing vaginal septum. A single left adnexal cyst lesion with blood products was suggestive of an endometriotic cyst. Additionally, the left kidney was absent. A uterine didelphys with left hemivagina obstruction, hematometra, hematocolpos, and the ipsilateral ovarian endometriotic cyst was diagnosed. A final diagnosis of OHVIRA syndrome or HWWS was made, considering that she had no left kidney.MRI is a suitable diagnostic tool for precise anatomical delineation of the uterus, cervix, and vagina in uterovaginal disorders such as OHVIRA syndrome. MRI can also properly evaluate endometriosis and adhesion.
    Matched MeSH terms: Urogenital Abnormalities/complications; Urogenital Abnormalities/diagnosis
  20. Gopal D, Telang A, Telang LA, Loganathan K, Reddy BT
    J Clin Diagn Res, 2015 May;9(5):ZD21-2.
    PMID: 26155582 DOI: 10.7860/JCDR/2015/12604.5915
    Nasopalatine duct cyst ( NPDC) is described as most common non-odontogenic developmental cyst of the jaws. Despite being common, its clinical and radiographic presentation could be varied and it can sometimes be a diagnostic challenge. This paper presents an unusual case of an infected NPDC associated with an impacted inverted mesiodens and a history of trauma that misled the clinical diagnosis.
    Matched MeSH terms: Jaw Abnormalities
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