Hyperostosis Frontalis Interna is characterized by the thickening of the frontal bone of the skull. It is not clear that this disorder is actually rare. Some clinicians. Hyperostosis frontalis interna is characterised by benign overgrowth of the inner table of the frontal bone. It is seen most commonly in older females. The etiology . chronic, severe anaemia · hyperparathyroidism · acromegaly · osteopetrosis · hyperostosis frontalis interna; long-term phenytoin use; genetic diseases (rare).
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Synonyms or Alternate Spellings: Galactorrhea is a condition in which there is a spontaneous flow of milk from the nipple. Other treatment is symptomatic and supportive.
Myotonic Dystrophy is an inherited disorder involving the muscles, vision, and endocrine glands. The importance of this condition stems mainly from the necessity of not mistaking it for pathology. Unable to process the form.
Camurati-Engelmann disease Case 7: They are not necessary for a differential diagnosis:. Hershkovitz I, et al.
Years Published, Facial deformities are often present at birth and may progress with time. Together we are strong. This alteration can occur in isolation or together with neuropsychiatric symptoms, metabolic and endocrine manifestations which together form the Morgagni-Stewart-Morel syndrome.
Hyperostosis Frontalis Interna – NORD (National Organization for Rare Disorders)
Central Nervous SystemMusculoskeletal. Genetic counseling may be of benefit for patients and their families. Articles Cases Courses Quiz. His powerful and sweet voice became legendary.
Case 2 Case 2. It can cause mental deficiency and loss of hair. There are no known cases of male-to-male father to son transmission.
Case 5 Case 5. Comparisons may be useful for a differential diagnosis: They are not necessary for a differential diagnosis: Hyperostosis frontalis interna HFI.
Hyperostosis frontalis interna
In spite of its bad preservation state, the skeleton displayed some interesting characteristics hiperoztosis are probably related to the effects of castration, including long limb-bones, persistence of epiphyseal lines and osteoporosis.
Case 4 Case 4. Other conditions that may be found in patients with this disorder are: Human traits, including the classic genetic diseases, are the product of the interaction of two genes, one received from the father and one from the mother.
About Blog Go ad-free. Am J Phys Anthropol. The following disorders have been found in association with Hyperostosis Frontalis Interna. Increased serum alkaline phosphatase and elevated serum calcium may occur.
Differential Diagnosis The differential is that of hyperostosis of the skull and includes: In hiperostksis were performed imaging of the skull where was observed the presence of extensive hyperostosis frontalis interna, cortical atrophy and a left thalamic lacunar infarction. Chaljub G, et al.
[Morgagni-Stewart-Morel syndrome. Case report and review of the literature].
Symptoms of the following disorders can be similar to those of Hyperostosis Frontalis Interna. Hyperostosis Frontalis Interna has been found in multiple generations iinterna that the disorder may be inherited as a dominant trait. As a result, scientists feel that this condition may be much more prevalent than suspected, but often goes undetected. Hyperostosis associated with meningioma of the cranial base: