PPT-A case of immotile cilia syndrome

Prof DR MNATARAJAN MD DRSYED BAHAVUDEEN HUSSAINI MD DNB DR VALLI DEVI MD Presentor P Muthukrishnan COMPLAINTS 42 year old male came with complaints of cough with expectoration 1 month. By Kevin Partlow, Neil Perry, and Chris . Paszkiewicz. Cilia and Flagella. Cilia-numerous minute hair like organelles. Flagella-identical to the cilia but there is less of them and they are smaller. Location and Functions. Chermak. Cilia Function. Cilia are hair-like organelles located on the outside of eukaryotic cells.. There are motile cilia and non-motile cilia.. Motile cilia move in a wave-like motion to move particles across the surface of the cell, or to allow unicellular organisms to move.. Jonathan Timothy . Adi. What are Flagella and Cilia?. Flagella and Cilia are the locomotion appendages of unicellular Eukaryotes. Basically they are the limbs of cells!. They can act like . legs, moving from place to place.. Case of the . Month . 15. September 2016. What is your diagnosis ?. History. : . 19-yr-old male patient referred to our department for preoperative thoracic imaging.. Physical Examination: healthy, . Dr. . D.Y.Patil. Medical College & Hospital. Pimpri. , . Pune. 12year , Female. c/o Headache * 2 weeks. Worsened on forward bending. Associated with vertigo and vomiting. No history of fever, seizures or visual symptoms. 201 Abstract:Cornelia de-Lange syndrome is characterized bydistinctive facial dysmorphism, primordial short stature,hirsutism, and upper limb reduction defects that range fromsubtle phalangeal abnorma Int J Anat Var Vol 12 No 3 Sep 2019 3DISCUSSIONBuschke-Ollendorff syndrome is a hereditary disease that affects the skin and bones, and is characterized by small spots of nodular opacity, called osteo J emds .com J . Evolution Med . Dent . Sci ./ eISSN - 2278 - 4802, pISSN - 2278 - 4748/ Vol. 8 / Issue 20 / May 20 , 201 9 Page 1682 PARRY ROMBERG SYNDROME - A CASE REPORT Dipu Bhuyan 1 , Upasa Nurul AM et al . ; , November 201 5 ; 3 ( 1 1 ): 10 9 5 - 10 9 8 Available Online: http://saspjournals.com/sjmcr 1095 Scholars Journal of Medical Case Reports ISSN 2347 - 6559 (Online) Sch J Med 1231 IntroductionSjogren-Larsson Syndrome (SLS) is a rare autosomal recessive, neurocutaneous disorder. is rare syndrome harbors mutations in the ALDH3A2 gene located on chromosome 17p11.2 [1].Ab CNS Gliosis not Neoplasia in Kabuki Syndrome: A Case Report of a Brain ‘Tumor’ Honey CM *1 , Cheng J 2 , Sulistyanto A 3 , Heran MKS 4 , Schutz P 5 and Hukin J 6 1 Department of Surgery, S  Article Waardenburg Syndrome: A Report of Two Familial Case Series Safal Khanal, B.Optom, Southwestern University, Cebu City, Philippines Pragati Gautam, MD, BP Koirala Lions Center for Ophthal &RS\ULJKWE\)DUKDQD7DKVHHQ7DMHWDO7KLVLVDQRSHQDFFHVVDUWLFOHGLVWULEXWHGXQGHUWKHWHUPV for . anti-fouling . surfaces. Shuaizhong Zhang. 1,2. , Ye Wang. 1. and Jaap den Toonder. 1. S.Zhang1@tue.nl. 1. Eindhoven University of Technology, the Netherlands . 2. China Scholarship Council, the People’s Republic of China.