haematobium
hematobium

The genome of Schistosoma haematobium has been reported.

S. haematobium infection probably also causes mucosal bleeding and inflammation.

Schistosoma intercalatum's life cycle is very similar to that of S. haematobium, except for some key differences.

Bilharz wrote a paper in 1856 describing the worms more fully and he named them Distoma haematobium.

It can be used to treat schistosomiasis caused by Schistoma haematobium but is no longer commercially available.

The genus has been divided into four groups - indicum, japonicum, haematobium and mansoni.

Urinary filtration or dipsticks are insensitive indicators for genital S. haematobium.

Artesunate is also efficient in reducing egg production in Schistosoma haematobium infection.

Studies have shown the relationship between S. haematobium infection and the development of squamous cell carcinoma of the bladder.

The tiny Bulinus snails are hosts for Schistosoma haematobium.

Mucosal grainy, sandy patches seem to be pathognomonic for S. haematobium infection in the female genitals.

"Resistance of B. (P.) nasutus productus to infection by S. haematobium".

The infectious agent (one of five species of flatworms, Schistosoma haematobium) is transmitted via tainted water.

Investigation of S. haematobium should also include a pelvic x-ray as bladder wall calcification is highly characteristic of chronic infection.

"Development of S. haematobium in Bulinus (P.) nasutus.

This species is an intermediate host for Schistosoma curassoni and for Schistosoma haematobium.

The parasites that cause schistosomiasis (bilharzia), especially S. haematobium, can cause bladder cancer and cancer at other sites.

Also, in 1851, during an autopsy, he discovered the trematode worm that is the cause of urinary schistosomiasis, initially naming it Distomum haematobium.

Inflammation of the genitals due to S. haematobium may contribute to the propagation of HIV.

The crushed biopsy of genital tissue is considered the gold standard for the parasitological diagnosis of genital S. haematobium.

Risks for squamous cell tumors in the bladder include indwelling catheters [38,39] and S. haematobium cystitis.

Post mortem studies and histopathological material from surgery in the reproductive tract have shown that S. haematobium may be distributed in all the pelvic organs.

Urinary schistosomiasis, a disease caused by the digenean trematode Schistosoma haematobium, has been implicated in the development of vesical calculi.

While crosses with S. mansoni give no viable offspring, the pairing with a male S. haematobium will result in a hybrid organism.

Most hybrids will have a diluted genome that is more closely related to S. haematobium, helping to bring about a decline in S. intercalatum populations.