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10.1111/j.1346-8138.2005.tb00870.x http://scihub22266oqcxt.onion/10.1111/j.1346-8138.2005.tb00870.x 16361753!ä!16361753 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=16361753&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Dermatol 2005 ; 32 (11): 909-13 Nephropedia Template TP {{tp|p=16361753|t=2005. Cardio-facio-cutaneous syndrome: two cases in the same generation |pdf=|usr=}}{{16361753}} gab.com Text Cardio-facio-cutaneous syndrome: two cases in the same generation JO: J Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=16361753 #FOAvip A 4-year-old Japanese boy, the youngest of three brothers, presented with ichthyosiform hyperkeratosis over his whole body, eczematous erythema with partial desquamation and erosion on the flexor side of the joints of extremities, the fossa axillaries, and the genital and buttock regions, and total hair loss on the scalp and the absence of eyebrows and eyelashes. In addition to the ichthyotic eruptions and hair abnormalities, he also had a ventricular septal defect, mental retardation, growth retardation, characteristic facial features such as a depressed nasal bridge, low-set ears, and ocular hypertelorism; therefore, he was diagnosed with cardio-facio-cutaneous (CFC) syndrome. The patient's family did not have a history of consanguineous marriage. The parents and the eldest son were healthy. However, the second son, also born with ichthyosiform hyperkeratosis over his whole body, total hair loss on the scalp, myocardial deficiency, mental retardation, growth retardation, and characteristic facial features, had died of pneumonia and sepsis at the age of 1.5 years. Because the middle brother had the same disease, the present case is considered to be a rare case of CFC syndrome with in a single generation. Twit Text FOAVip Cardio-facio-cutaneous syndrome: two cases in the same generation ????J Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=16361753 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=16361753 #FOAvip English Wikipedia <ref>{{Cite pmid|16361753}}</ref> Cardio-facio-cutaneous syndrome: two cases in the same generation #MMPMID16361753 Ikeda H; Hatamochi A; Okita H; Yamazaki S J Dermatol 2005[Nov]; 32 (11): 909-13 PMID16361753show ga A 4-year-old Japanese boy, the youngest of three brothers, presented with ichthyosiform hyperkeratosis over his whole body, eczematous erythema with partial desquamation and erosion on the flexor side of the joints of extremities, the fossa axillaries, and the genital and buttock regions, and total hair loss on the scalp and the absence of eyebrows and eyelashes. In addition to the ichthyotic eruptions and hair abnormalities, he also had a ventricular septal defect, mental retardation, growth retardation, characteristic facial features such as a depressed nasal bridge, low-set ears, and ocular hypertelorism; therefore, he was diagnosed with cardio-facio-cutaneous (CFC) syndrome. The patient's family did not have a history of consanguineous marriage. The parents and the eldest son were healthy. However, the second son, also born with ichthyosiform hyperkeratosis over his whole body, total hair loss on the scalp, myocardial deficiency, mental retardation, growth retardation, and characteristic facial features, had died of pneumonia and sepsis at the age of 1.5 years. Because the middle brother had the same disease, the present case is considered to be a rare case of CFC syndrome with in a single generation. |Alopecia/genetics/*pathology[MESH] |Child, Preschool[MESH] |Facies[MESH] |Heart Septal Defects, Ventricular/genetics/pathology[MESH] |Humans[MESH] |Intellectual Disability/genetics/pathology[MESH] |Keratosis/genetics/*pathology[MESH] |Male[MESH] |Pedigree[MESH]Cardio-facio-cutaneous syndrome: two cases in the same generation (epmc).pdf DeepDyve Pubget Overpricing