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10.1055/s-2008-1046600 http://scihub22266oqcxt.onion/10.1055/s-2008-1046600 8051913!ä!8051913 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Klin+Padiatr 1994 ; 206 (3): 181-3 Nephropedia Template TP {{tp|p=8051913|t=1994. Das Cardio-Facio-Cutane Syndrom--Blickdiagnose eines seltenen Syndroms |pdf=|usr=}}{{8051913}} gab.com Text Das Cardio-Facio-Cutane Syndrom--Blickdiagnose eines seltenen Syndroms JO: Klin Padiatr http://www.kidney.de/pget.php?&tw=1&pmid=8051913 #FOAvip This is a report of a case of cardio-facio-cutaneous (CFC) syndrome in a three-year-old boy. Apart from obvious signs of retardation in his mental and motor development, the child was conspicuous through his short stature, relative macrocephaly, vitium cordis, pendular nystagmus and ptosis and optic atrophy on both sides. The typically dysmorphic facial features that characterize this syndrome such as high forehead, biparietal impression, downward slant of the palpebral fissures, hypoplastic supraorbital ridges, depressed nasal bridge, high palate, and dysplasia of the ears, were particularly marked in this case. The hands and feet were plump, the skin rather thick, and the hair sparse and very curly. A chromosome analysis as well as metabolism tests proved normal. Until now there have been 27 reports of such cases in medical literature. Twit Text FOAVip Das Cardio-Facio-Cutane Syndrom--Blickdiagnose eines seltenen Syndroms ????Klin Padiatr http://www.kidney.de/pget.php?&tw=1&pmid=8051913 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=8051913 #FOAvip English Wikipedia <ref>{{Cite pmid|8051913}}</ref> Das Cardio-Facio-Cutane Syndrom--Blickdiagnose eines seltenen Syndroms #MMPMID8051913 Haas K; Schoning M; Enders H Klin Padiatr 1994[May]; 206 (3): 181-3 PMID8051913show ga This is a report of a case of cardio-facio-cutaneous (CFC) syndrome in a three-year-old boy. Apart from obvious signs of retardation in his mental and motor development, the child was conspicuous through his short stature, relative macrocephaly, vitium cordis, pendular nystagmus and ptosis and optic atrophy on both sides. The typically dysmorphic facial features that characterize this syndrome such as high forehead, biparietal impression, downward slant of the palpebral fissures, hypoplastic supraorbital ridges, depressed nasal bridge, high palate, and dysplasia of the ears, were particularly marked in this case. The hands and feet were plump, the skin rather thick, and the hair sparse and very curly. A chromosome analysis as well as metabolism tests proved normal. Until now there have been 27 reports of such cases in medical literature. |*Skin Abnormalities[MESH] |Abnormalities, Multiple/*diagnosis/genetics[MESH] |Child, Preschool[MESH] |Dwarfism/diagnosis/genetics[MESH] |Ear, External/abnormalities[MESH] |Facial Bones/*abnormalities[MESH] |Hair/*abnormalities[MESH] |Heart Defects, Congenital/*diagnosis/genetics[MESH] |Humans[MESH] |Infant[MESH] |Intellectual Disability/diagnosis/genetics[MESH] |Male[MESH] |Skull/*abnormalities[MESH]Das Cardio-Facio-Cutane Syndrom--Blickdiagnose eines seltenen Syndroms(epmc).pdf DeepDyve Pubget Overpricing