Tuesday, February 2, 2010

- Metabolic cuases of Impotence.

Metabolic cuases of Impotence (erectile dysfunction).

"Rash"


Renal Failure.
Alcoholism.
Sickle cell disease
Hoemochromatosis.
Hepatic failure.
Hyperglycemia (D.M).

Dr Ibrahim

Monday, February 1, 2010

- Nematodes affecting skin and s.c tissue.


Nematodes affecting skin and subcutaenous tissue.

"Hook was old"


Hook worms(Ground itching).


Wuchereria Bancrofti,Wuchereria malayi(they cause Elephentiasis).
Ancylstoma caninum,Ancylstoma Brazilliense (they cause creeping eruption).
Strongyloides stercoralis (creeping eruption).




Onchocerca volvulus(Nodules and Elephentiasis).
Loa Loa (Calabar swelling).
Dracunculus medinensis(ulcer and cellulitis).

Dr Ibrahim

Friday, January 29, 2010

- Parasites affecting Heart.

Parasites affecting Heart
"Heart Team
Heterophyes heterophyes (Eggs)

Taenia solium (cysticercosis), 
Trichinella spiralis (Trichina capsule),
Trypanosoma cruzi (Leishmanial form),
Toxoplasma gondii (true tissue cyst).

Echinococcus granulosus (Hydatid cyst).
Acanthocheilonema perstans (Adult worm in the pericardium).
Mansonella ozzardi
(Adult worm in the pericardium).

or  Arabic students can use the word "Hatem"

Dr Ibrahim

Thursday, January 28, 2010

- Kallmann syndrome.

 Kallmann syndrome


- Def :- It is a rare X-linked recessive genetic disease which characterized by delayed or absent puberty and an impaired sense of smell, also referred as olfactogenital dysplasia.

- Kallmann syndrome is a form of secondary hypogonadism, reflecting that the primary cause of the defect in sex-hormone production lies within the pituitary and hypothalamus rather than a physical defect of the testes or ovaries.

- Kallmann syndrome was described in 1944 by Franz Josef Kallmann, a German-American geneticist.(1)(2)

- Incidence:-
It affects primarily males at an incidence of 1 out of 10,000 in a study of French conscripts.(3)
The male-to-female ratio ranges from 4:1 to 5:1.

- Cause:-
Mutations in the KAL1, FGFR1, PROKR2, and PROK2 genes cause Kallmann syndrome.
These genes play a role in the development of certain areas of the brain before birth. Although some of their specific functions are unclear, these genes appear to be involved in the formation and movement (migration) of a group of nerve cells that are specialized to process smells (olfactory neurons).(4)

- Synonyms:-
  • de Morsier’s syndrome II.
  • Morsier-Gauthier syndrome.
  • Kallmann-de Morsier syndrome.
  • Maestre-Kallmann-de Morsier syndrome.
  • Maestre de San Juan-Kallmann syndrome.
  • Maestre de San Juan-Kallmann-de Morsier syndrome.
  • anosmic hypogonadism.
  • anosmic idiopathic hypogonadotropic hypogonadism.
  • hypogonadotropic hypogonadism and anosmia.
  • hypogonadotropic hypogonadism-anosmia syndrome.

Wednesday, January 27, 2010

- Sertoli-cell-only syndrome (germinal cell aplasia).

Sertoli-cell-only syndrome (SCO)
-Def:- It is a condition in which only Sertoli cells line the seminiferous tubules of the testes and characterized by male sterility (due to azoospermia) without sexual abnormality.
- Synonyms:-
  • Del Castillo syndrome.
  • Germ cell aplasia.
-The etiology (1):-
  • Most causes of SCO syndrome are idiopathic. A congenital absence of germ cells due to failure of migration of gonocytes is theoretically possible.
  • Massive deletions in the azoospermia factor (AZF) region of the Y chromosome. found.
  • Exposure to chemicals and toxins may cause SCO; however, direct cause-and-effect relationships in humans have been difficult to document.
  • Klinefelter syndrome, 47 XXY, results in a characteristic biopsy appearance of SCO and Leydig cell hyperplasia.