Cerita Anas Syazni: February 2010

Friday, February 26, 2010

keras..keras..keras

Hampir dekat 2 minggu juga Anas selalu sgt mengeraskan badannya..susah nak pegang,susah nak bentuk balik badannya yang keras...mcm perah kain..ker sawan ..xtau dh nak ckp...bila dah keras,dia nangisla..sakit .kalau kita mgkin cam'tarik mengkarung'..

Berita yang gembira

9 Februari 2010,doktor genetik mengesahkan Anas tidak menghidapi penyakit 'menkes'.Leganya hati..lilitan kepala Anas juga bertambah sikit jer dalam 1 inci...hehehe..

sekarang Anas kerap menanggis dalam apa jua keadaan,baik lapar,panas,basah& sebagainya..berbanding dahulu banyak perkembangan.

Sedikit info tentang MENKES.
(1)berpunca dari bahan kimia di dalam badan kita yang mungkin kurang@lebih...selalunya iron...
(2)boleh diuji melalui darah dan urine...
(3)simptom2 fizikal...kulit putih,rambut keras,urat darah yg tidak kelihatan(pecah),sawan,muntah

Info Semasa

What is Ohtahara Syndrome?

Ohtahara syndrome is a neurological disorder characterized by seizures. The disorder affects newborns, usually within the first three months of life (most often within the first 10 days) in the form of epileptic seizures. Infants have primarily tonic seizures, but may also experience partial seizures, and rarely, myoclonic seizures. Ohtahara syndrome is most commonly caused by metabolic disorders or structural damage in the brain, although the cause or causes for many cases can’t be determined. Most infants with the disorder show significant underdevelopment of part or all of the cerebral hemispheres. The EEGs of infants with Ohtahara syndrome reveal a characteristic pattern of high voltage spike wave discharge followed by little activity. This pattern is known as “burst suppression.” Doctors have observed that boys are more often affected than girls.

Is there any treatment?

Antiepileptic drugs are used to control seizures, but are unfortunately not usually very effective for this disorder. Corticosteroids are occasionally helpful. In cases where there is a focal brain lesion (damage contained to one area of the brain) surgery may be beneficial. Other therapies are symptomatic and supportive.

What is the prognosis?

The course of Ohtahara syndrome is severely progressive. Seizures become more frequent, accompanied by physical and mental retardation. Some children will die in infancy; others will survive but be profoundly handicapped. As they grow, some children will progress into other epileptic disorders such as West syndrome and Lennox-Gestaut syndrome.

What are the symptoms?

The signs of Ohtahara syndrome are:

Tonic seizures (stiffening of the extremities);
Psychomotor development delay (delay in development of skills involving mental and motor development);
There may be later development of other neurological difficulties such as diplegia (spasticity and weakness in the legs), hemiplegia (spasticity and weakness of one side of the body), tetraplegia (spasticity and weakness of both sides of the body), ataxia (unsteady gait), or dystonia (abnormal movements with increased tone).