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Publications :

Publications List:

Ghada Y. El-Kamah , Mohamad A. El-darouti , Ahmad IS. Kotoury   Mostafa I. Mostafa. Farber disease overlapping with stiff skin syndrome: Expanding the spectrum. Egypt. J. Med. Hum. Genet. 10, 1: 97-104, 2009.

Afifi HH, Zaki  MS, El-Kamah  GY, El-Darouti M. “ Elejalde syndrome: Clinical and histological findings in an Egyptian male.”. Genetic Counseling .18,2: 179-188, 2007.

Pachyonychia congenita: treatment of the thickened nails and palmoplantar circumscribed callosities with urea 40% paste.
El-Darouti MA, Marzouk SA, Nabil N, Abdel-Halim MR, El-Komy MH, Abdel-Latif M.
J Eur Acad Dermatol Venereol. 2006 May;20(5):615-7

M.Abdallah, AB Zaghloul,A. Rashid, MA. Abdallah Kindler ,Weary,or Kindler -Weary syndrome, JEADV,2005, 19; supp1,oct ( poster) P05.78

Temtamy SA, El-Kamah Gh, Ismail S, Mazen I and El-Darouty M(2004): Report of four Egyptian cases representing two new rare types of Ehlers-Danlos syndrome. Journal of Arab Child. 15:91-111,2004.

Dawn H,Siegel,Adel B.Zaghloul,et al:Loss of Kindilin-1,a human homolog of the caneohabditis elegans actin-extracellular matrix linker protein UNC-112,causes Kindler syndrome.AM.J.Hum.Genet.73:174-187,2003

Clinical and genetic study of xeroderma pigmentosum.
al Rubaie SM, el Darouti MA.
Int J Dermatol. 1990 Mar;29(2):126-8.

 Papillon-Lefèvre syndrome. Successful treatment with oral retinoids in three patients.
el Darouti MA, Al Raubaie SM, Eiada MA.
Int J Dermatol. 1988 Jan-Feb;27(1):63-6.