Robinow syndrome and fusion of primary teeth
نویسندگان
چکیده
منابع مشابه
comparison of zoe and vitapex for canal treatment of necrotic primary teeth
چکیده ندارد.
15 صفحه اولUnusual traits associated with Robinow syndrome.
We report on some members of two unrelated families showing the characteristic features of Robinow syndrome. In a consanguineous Kuwaiti family, the index case with Robinow syndrome showed some unusual features including severe IUGR, laxity of ligaments, hyperextensible joints, redundant skin folds, severe normocytic anaemia, repeated infection, increased percentage of total T cells and CD4 pos...
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The Chediak-Higashi syndrome (CHS) is a rare hereditary fatal disease, if not treated. These changes are associated with various diseases and syndromes that mainly cause periodontal disease and thus the premature loss of teeth. This paper describes the monitoring of premature loss of primary teeth that began when the child was 5 years old. On presentation his teeth were mobile and there was a h...
متن کاملCase Report: Simultaneous Presence of Primary and Permanent Teeth
Although the delayed exfoliation of primary teeth among children is a common dental problem, simultaneous presence of primary teeth and corresponding successors is a rare feature in adults. This paper reports an unusual case in which both permanent teeth (molars, premolars, and canines) and primary teeth were present simultaneously. This report describes questions concerning...
متن کاملRobinow Syndrome: A Rare Case Report and Review of Literature
Robinow syndrome is an extremely rare genetic disorder. Short-limbed dwarfism, abnormalities in the head, face, and external genitalia, as well as vertebral defects comprise its distinct features. This disorder exists in dominant and recessive patterns. Patients with the dominant pattern exhibit moderate symptoms. More physical characteristics and skeletal abnormalities characterize the recessi...
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ژورنال
عنوان ژورنال: Contemporary Clinical Dentistry
سال: 2017
ISSN: 0976-237X
DOI: 10.4103/ccd.ccd_622_17