TITLE

Cleidocranial dysplasia

AUTHOR(S)
Dixit, Ramakant; Dixit, Kalpana; R., Paramez A.
PUB. DATE
July 2010
SOURCE
Lung India;Jul-Sep2010, Vol. 27 Issue 3, p176
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Cleidocranial dysplasia is a rare autosomal dominant condition with generalized dysplasia of bone, characterized by delayed closer of cranial sutures, hypoplastic or aplastic clavicles, short stature, dental abnormalities and a variety of other skeletal abnormalities. We present a seven-year-old female child presenting with classical features of cleidocranial dysplasia.
ACCESSION #
53290983

 

Related Articles

  • Cleidocranial Dysplasia - A case report. Reddy, E. Siva Prasad // Journal of Advanced Dental Research;May-Aug2011, Vol. 2 Issue 2, p37 

    Cleidocranial dysplasia is an autosomal dominant disorder with skeletal dysplasia. The dental manifestations are mainly delayed exfoliation of primary teeth and delayed eruption of permanent teeth with multiple impacted supernumeraries, it is noteworthy that the case of 20 year old girl reported...

  • Surgical Treatment of Trigonocephaly. AKAN, Mithat; AVCI, Gülden; SİLAV, Gökalp; AKÖZ, Tayfun; ELMACI, İlhan // Journal of Neurological Sciences;2011, Vol. 28 Issue 1, p42 

    No abstract available.

  • A subacute epidural haematoma extending over the occipital region and posterior cranial fossa due to a laceration in the transverse sinus. Inoue, Hiromasa; Nakagawa, Yasuhisa; Ikemura, Mayumi; Shinone, Kotaro; Okada, Kana; Nata, Masayuki // International Journal of Legal Medicine;May2012, Vol. 126 Issue 3, p467 

    A 6-year-old male was found dead on his stomach with massive reddish vomiting from his mouth and nose. Postmortem cranial CT revealed an epidural haematoma in the left occipital region, but the cause and origin of the haematoma were unclear. An autopsy revealed that the epidural haematoma...

  • Trichorhinophalangeal syndrome II, expanding the clinical spectrum. Shawky, Rabah M.; Elkhalek, Heba Salah Abd; Elghawaby, Ahmed E. S.; Mohammad, Shaimaa Abdelsattar; Seifeldin, Neveen S. // Egyptian Journal of Medical Human Genetics;2015, Vol. 16 Issue 1, p89 

    We report a 4.5 year old Egyptian male child, fourth in the order of birth of healthy remote consanguineous parents. He has typical facial as well as skeletal features of Trichorhinophalangeal syndrome (TRPS) II. The facial features included bilateral downward slanting palpebral fissures,...

  • Stafne's Defect with Buccal Cortical Expansion: A Case Report. Campos, Paulo Sérgio Flores; Carvalho Oliveira, José Aloysio; Araújo Dantas, Janaina; de Melo, Daniela Pita; Pena, Nilson; Nogueira Santos, Luís Antônio; Crusoé-Rebello, Iêda Margarida Rocha // International Journal of Dentistry;2010, p1 

    A rare case of Stafne's bone cavity, type III-G, is reported in a 49-year-old male patient who had been referred to a private clinic for a routine evaluation. The final diagnosis was based on computed tomography. Scintigraphy played a fundamental role in determining the most likely etiology.

  • Common dental features and craniofacial development of three siblings with Ter Haar syndrome. Parker, K.; Pabla, R.; Hay, N.; Ayliffe, P. // European Archives of Paediatric Dentistry (Springer Science & Bu;Feb2014, Vol. 15 Issue 1, p59 

    Background: Ter Haar syndrome is a rare genetic syndrome with <30 cases reported worldwide. There is nothing within the published literature regarding the dental development and dental features of these patients. Case report: This case series examines three patients with Ter Haar syndrome and...

  • A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2. Masaki Takagi; Hiroko Yagi; Yoshie Nakamura; Hiroyuki Shinohara; Ryojun Takeda; Aya Shimada; Gen Nishimura; Yukihiro Hasegawa // Clinical Pediatric Endocrinology;Jul2015, Vol. 24 Issue 3, p139 

    The article describes the case of q 15-year-old Japanese male with spondyloepiphyseal dysplasia tarda (SEDT) due to a novel intragenic deletion of trafficking protein particle complex 2 (TRAPPC2). Topics discussed include the patient's pedigree and longitudinal growth record, radiographs of his...

  • Multi-detector thoracic CT findings in cerebro-costo-mandibular syndrome: rib gaps and failure of costo-vertebral separation. Watson, Tom; Arthurs, Owen; Muthialu, Nagarajan; Calder, Alistair // Skeletal Radiology;Feb2014, Vol. 43 Issue 2, p263 

    Cerebro-costo-mandibular syndrome (CCMS) describes a triad of mandibular hypoplasia, brain dysfunction and posterior rib defects ('rib gaps'). We present the CT imaging for a 2-year-old girl with CCMS that highlights the rib gap defects and shows absent transverse processes with abnormal fusion...

  • Ribbing disease (multiple diaphyseal sclerosis): a case report and literature review. Zhang, Lin; Jiang, Wei; Li, Xue; Yuan, Jing; Yang, Hui // Journal of Orthopaedic Science;Nov2011, Vol. 16 Issue 6, p828 

    The article describes the case of a 31-year-old female patient who was diagnosed with ribbing disease. Her chief complaint was progressive aching pain in her left thigh following physical activity. An increase in the diaphyseal density and left femur thickness was detected via radiographs. She...

Share

Read the Article

Courtesy of VIRGINIA BEACH PUBLIC LIBRARY AND SYSTEM

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics