Monday, November 28, 2011

Sebarkan Bahagia ( Blog Fatimah Syarha ): Karier Wanita dalam Fiqih al-Qaradhawi

Sebarkan Bahagia ( Blog Fatimah Syarha ): Karier Wanita dalam Fiqih al-Qaradhawi: "Abang, indah melukis impian masa depan bersamamu :)" “Abang nak tahu impian Sayang untuk para bidadari kita… Sayang impikan bidadari-bid...

Sunday, November 27, 2011

Saturday, November 26, 2011

Salam Maal Hijrah 1433 ...

Dalam kesibukan mengejar pusingan roda dunia,sedar-sedar malam ni telah pun memasuki tahun baru islam..(26/11/2011)..Rasanya seperti baru semalam doa awal tahun dibacakan..

Tahun baru sudah bermula,tetapi masih banyak azam tahun lpas yg x dpt Dipenuhi...memang betul..demi masa,sesungguhnya manusia kerugian...
Semoga azam thun lpas dpt dilaksanakan pada tahun ini ,begitu juga dgn azam thun baru ni..

disini saya kongsikan doa tahun baru...yg perlu dibaca selepas maghrib...semoga dpt dijadikaN Panduan..

SEMOGA CINTA ALLAH MENGIRINGI SETIAP HEMBUSAN NAFAS .... DAN DEGUPAN JANTUNG KITA..AMIN...

Monday, November 21, 2011

Morquio syndrome

21/11/11 ,i wAS placed in orthopaedic ot ..so,as usual,before start working..i'll check the orthopaedic list for operation today..then,something draw my attention..MORQUIO SYNDROME..hurmm..the first things that running in my head is..what is this?? how this syndrome could effect this patient?? plus,this patient having difficulty in intubtion.. i believe..many of nurses out there didn't known what this morquio syndrome..so,,i'm happy to sharing with all the my friends especially all nurses bout this disease...'sharing is caring'..isn't ??

Morquio syndrome

The individual on the front of the scooter is 19 y

Mucopolysaccharidosis type IVA; Galactosamine-6-sulfatase deficiency; Mucopolysaccharidosis type IVB; Beta galactosidase deficiency; MPS IV

Last reviewed: May 15, 2011.

Morquio syndrome is an inherited disease of metabolism in which the body is missing or doesn't have enough of a substance needed to break down long chains of sugar molecules called glycosaminoglycans (formerly called mucopolysaccharides).

The syndrome belongs to a group of diseases called mucopolysaccharidoses (MPS). Specifically, it is known as MPS IV.

Causes, incidence, and risk factors

Morquio syndrome is an autosomal recessive trait. That means both your parents must pass you the defective gene in order for you to get this disease.

There are two forms of Morquio syndrome: Type A and Type B.

Persons with Type A do not have a substance (enzyme) called galactosamine-6-sulfatase.
Persons with Type B do not produce enough of an enzyme called beta-galactosidase.

The body needs these enzymes to break down a long strand of sugar molecules called the keratan sulfate sugar chain. In both types, abnormally large amounts of glycosaminoglycans build up in the body and brain, which can damage organs.

The syndrome is estimated to occur in 1 of every 200,000 births. Symptoms usually start between ages 1 and 3. A family history of the syndrome raises one's risk for the condition.

Symptoms

Abnormal development of bones, including the spine
Bell-shaped chest with ribs flared out at the bottom
Coarse facial features
Hypermobile joints
Knock-knees
Large head (macrocephaly)
Short stature with a particularly short trunk
Widely spaced teeth

Signs and tests

The doctor will perform a physical examination. Examination and testing may reveal:

Abnormal curvature of the spine (kyphoscoliosis)
Cloudy cornea
Heart murmur (aortic regurgitation)
Inguinal hernia
Liver enlargement
Loss of nerve function below the neck
Short stature (especially short trunk)

Urine tests are usually done first. These tests may show extra mucopolysaccharides, but they can't determine the specific form of MPS.

Other tests may include:

Blood culture
Echocardiogram
Genetic testing
Hearing test
Slit-lamp eye exam
Skin fibroblast culture
X-rays of the long bones, ribs, and spine

Persons with Morquio syndrome should have MRI of the lower skull and upper neck to determine if the upper vertebrae are underdeveloped.

Treatment

There is no specific treatment for Morquio syndrome. Researchers are currently testing a possible treatment involving enzyme replacement.

Symptoms are treated as they occur. A spinal fusion may prevent permanent spinal cord injury in persons whose neck bones are underdeveloped.

Support Groups

National MPS Society --www.mpssociety.org

Expectations (prognosis)

Cognitive (thinking) function is usually normal in patients with Morquio syndrome.

Bone problems can lead to significant complications. For example, the small bones at the top of the neck may slip and damage the spinal cord, causing paralysis. Surgery to correct such problems should be done if possible.

Heart (cardiac) complications may lead to death.

Complications

Breathing problems
Heart failure
Spinal cord damage and possible paralysis
Vision problems
Walking problems related to abnormal curvature of the spine and other bone problems

Calling your health care provider

Call your health care provider if symptoms of Morquio syndrome occur.

Prevention

Genetic counseling is recommended for prospective parents with a family history of Morquio syndrome. Counseling is also recommended for families who have a child with Morquio syndrome, to help them understand the condition and possible treatments.

References

National Institute of Neurological Disorders and Stroke. Mucolipidoses Fact Sheet. Office of Communications and Public Liaison. Bethesda, MD; Publication No. 03-5115. February 13, 2007.

PubMed Health

Sunday, November 20, 2011

Doa elak dicabul atau dirogol.

Hari ini ,semakin ramai kaum hawa dan kanak-kanak yg mnjadi mangsa kerakusan manusia yg berajakan nafsu dalam jiwa..

Maka di sini, saya kongsikan doa dari hadis sohih pelindung setiap kali keluar rumah . Iaitu :-

بِسْمِ اللَّهِ الذي لَا يَضُرُّ مع اسْمِهِ شَيْءٌ

في الأرض ولا في السَّمَاءِ وهو السَّمِيعُ

الْعَلِيمُ

DALAM sebutan rumi : BISMILLAH ALLAZI LA YADURRU MA’ASMIHI SYAIUN FIL ARDI WA LA FIS SAMAIE , WAHUWAS SAMI’UL ‘ALIM

Ertinya : Rasulullah s.a.w didengari berkata sesiapa yang berdoa : “Dengan nama Allah yang tiada dimudaratkan sesuatu apapun dengan namaNya samada di bumi dan di langit, dan Dialah maha mendengar dan maha mengetahui”

sebanyak 3 kali, maka ia tidak ditimpa kesusahan bala dan musibah sehinggalah subuh esoknya, dan barangsiapa membacanya ketika subuh 3 kali, ia tidak ditimpa kesusahan bala dan musibah sehingga petangnya” ( Riwayat Abu Daud, 4/323 ; At-Tirmidizi, 5/465 dan Ahmad ; Tirmizi : Hasan – Teks doa berwarna Merah Syeikh Syuaib ; Hasan)

Ingin saya utarakan satu lagi doa sohih yang dibaca oleh isteri Nabi Ibrahim a.s (iaitu Siti Sarah) yang menyebabkan para lelaki zalim termasuk rajanya melarikan diri, saya sertakan sekali sumber rujukannya dari hadis Nabi s.a.w.

اللّهُمَّ اِنْ كُنْتَ تَعْلَمُ اني آمَنْتُ بِكَ وَبِرَسُولِكَ وَأَحْصَنْتُ فرجي إِلاَّ على زوجي فَلاَ تُسَلِّطْ عَلَىَّ الْكَافِرَ

DALAM SEBUTAN RUMI : ALLAHUMMA IN KUNTA TA’LAMU INNI AAMANTU BIKA, WA BIRASULIKA WA AHSONTU FARJI ILLA ‘ALA ZAWJI FALA TUSALLIT ‘ALAYYA AL-KAFIR WA AZ-ZALIM

Ertinya : Ya Allah, jika engkau mengetahui bahawa aku beriman kepada Mu dan Rasul Mu, dan aku menjaga kehormatanku hanya untuk suamiku, maka lindungilah aku daripada dikuasai oleh orang-orang kafir dan zalim”( Riwayat Al-Bukhari, no 2104, 2/722 ; Sunan Al-Baihaqi, 5/97; Musnad ahmad, 2/403 ; Fath Al-Bari, 6/393; Umdat Al-Qari, 12/30 ; Sohih )

Semoga ia dapat dihafaz dan di amalkan oleh semua wanita Muslimah, Cuma jangan lupa bahawa doa ini bersoifat tawassul dengan amal soleh anda, iaitu apabila diikat dengan imannya dengan Allah s.w.t dan RasulNya dan telah dijaga kehormatannya dan sudah tentu auratnya.

Justeru, seolah-olah kemaqbulan doa ini juga diikat tentang kewajiban untuk beriman dengan Allah dan rasulNya dan menutup aurat anda. Tanpanya, doa ini masih amat digalakkan untuk dilakukan, cuma jaminan seolah-olah lebih pasti bagi yang apa yang dikatanya (dalam doa ini) menepati apa yang sebenarnya penampilan fizikal anda.

Wallahua'lam via coretan hamba