نتایج جستجو برای: cutis laxa
تعداد نتایج: 2419 فیلتر نتایج به سال:
Cutis laxa is a term that refers to markedly loose skin that is not hyperelastic. It is regarded as a genetically heterogeneous group of diseases and is presently divided into five types. We report a male patient with type II autosomal recessive disease. The patient was the third child of first-cousin consanguineous, healthy parents. His two siblings died a few hours after birth. One of the sib...
the aim of the this work was to determine the finger patterns, finger ridge count (frc), total finger ridge count (tfrc), and asymmetry of finger ridge count (afrc) of an iranian girl (aged 13 years) affected with congenital cutis laxa (ccl).the fingerprints of the first phalanx of both hands were taken by using the standard method (stamp ink). the fingerprints were classified according to the ...
Congenital leukemia is a rare disease with particular biological and clinical characteristics, which differs from those of older children. Its prognosis is generally poor. Its clinical manifestation may vary (hyperleukocytosis, thrombocytopenia, organomegaly) and some patients can develop cutaneous infiltration by leukemic cells (leukemia cutis). We describe a dysmorphic patient with thrombocyt...
Cutis laxa is a rare disease, related to loss of skin elasticity, which can be hereditary or acquired, with without associated visceral damage. It marked by great psychological and social repercussions. The purpose this paper highlight particular cause neonatal occlusion: cutis laxa. We report new observation about case hospitalized in the pediatric department at Mohammed V hospital Tangier, ad...
Acquired cutis laxa is an uncommon disorder sometimes associated with monoclonal gammopathy and multiple myeloma, although the mechanism of this link is unclear. We report here a case of a 34-year-old man with generalized acquired cutis laxa and monoclonal light chain disease with renal and neurological involvement. Electron microscopy examination of a skin sample revealed shortened and fragmen...
ABSTRACT Cutis laxa is a congenital disorder transmitted as autosomal ressesive and dominate trait. This disorder has an acquired form that develops after febrile illness or skin inflammatory fisease. A 5 month old girl with generalized loose skin and these facial features including a hooked nose with everted nosetrils, long filtrom, high arch palate, wide fontanels, hypertelorism, e...
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal recessive and x-linked recessive patterns have been described in the inherited forms. Acquired forms of this disease have been associated with a prev...
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