نتایج جستجو برای: atrophia maculosa varioliformis cutis
تعداد نتایج: 2604 فیلتر نتایج به سال:
Pond populations in Cape Cod described as Persicaria puritanorum (≡ Polygonum puritanorum) have been treated by recent authors as a synonym of P. maculosa (≡ Polygonum persicaria) based on gross morphology. However, consistent differences in leaf and inflorescence features raise the question as to whether this is an extreme phenotype of P. maculosa, an ecotype of that species, or a distinct tax...
Congenital cutis laxa is an exceptional condition. No large scale pedigree has been reported from Iran. We report a family with 106 members with two members affected with cutis laxa. Our cases were two patients (male and female) with pre- and postnatal growth retardation, cutis laxa, characteristic facies and other manifestations which proved that they were affected with cutis laxa. Their ...
congenital cutis laxa is an exceptional condition. no large scale pedigree has been reported from iran. we report a family with 106 members with two members affected with cutis laxa. our cases were two patients (male and female) with pre- and postnatal growth retardation, cutis laxa, characteristic facies and other manifestations which proved that they were affected with cutis laxa. their famil...
OBJECTIVE This research was performed to investigate the efficacy of complex rehabilitation combined with pharmacopuncture treatment for the children with neuromotor system diseases. METHODS Fifty (50) patients aged from 5 to 15 yr old were compared. Twenty (20) patients received conventional treatments and complex rehabilitation as a control group, and fifty (50) patients received complex re...
BACKGROUND The Pelger-Huet anomaly dominantly is a rare and benign inherited defect of terminal neutrophil differentiation. Although neutrophil migration may be minimally impaired, granulocytes function is otherwise normal association abnormalities such as ocular, musculoskeletal are reported very rare. Case Presentation : An eight year-old boy with good consciousness but severe muscular atroph...
The burbot, Lota lota (Teleostei: Gadidae), has a holarctic distribution, with one subspecies (Lota lota lota) living in the lakes and rivers of the Palaearctic and northwestern North America and the other (Lota lota maculosa) living in the Nearctic (except the northwest). We analysed nine microsatellite loci and the mitochondrial DNA control region of 350 burbot sampled across North America to...
cutis laxa is an acquired or inherited condition characterized by redundant, sagging and inelastic skin. the inherited form is heterogeneous condition with autosomal dominant, autosomal recessive and x-linked inheritance. autosomal dominant cutis laxa is divided into three types, type i, ii and iii and the responsible genes are eln, fbln5 and aldh18a1 respectively. an x-linked form of cutis l...
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