1st child-Airis fatiha

Lilypie - Personal pictureLilypie Fourth Birthday tickers

2nd child - Irdhina Sofia

Lilypie Second Birthday tickers

Tuesday, August 25, 2009

Kisah kanak-kanak terkecil






Salam semua,


Dalam kesibukan dan kekusyukan kita menjalankan ibadah, ni just nak share cerita yg aku dapat daripada email pasal kenadie kanak2 terkecil...sebesar bayi je..lahir tahun 2003.Patutnya skrg dah berumur 6tahun la kan..Ala ni mcm kes yg pernah jadi dkt malaysia jugak.igt x?nama budak tu dah lupa tp pernah masuk paper dan tv.hurm macam2 kan?


Kenadie Jourdin-Bromley, known around the world as "the littlest angel", was born Feb.13, 2003, weighing just 2 lbs, 8 ounces. Doctors were at a loss as to why she was born so small and told her parents this little miracle baby likely wouldn't live through the night. But she did.
She continued to defy doctors expectations and at the age of 8 months, Kenadie was finally diagnosed with primordial dwarfism, a genetic condition that is believed to affect only about 100 people in the world. She isn't expected to grow past about 30 inches or weigh more than 8 pounds.
Nearing the age of four, Kenadie now walks, runs, laughs, smiles and is beginning to talk. But, perhaps more importantly, it's the way Kenadie makes people feel that is her strongest achievement.
She may be small but no one would argue that this little girl has an enormous effect on people throughout the world.


apa dia penyakit primordial dwarfism ?
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Primordial dwarfism is a rare form of dwarfism that results in a smaller body size in all stages of life beginning from before birth. More specifically, primordial dwarfism is a diagnostic category including specific types of profoundly proportionate dwarfism, in which individuals are extremely small for their age, even as a fetus. Most individuals with primordial dwarfism are not diagnosed until they are about 3 years of age.

Medical professionals typically diagnose the fetus as being small for the gestational age, or as having intrauterine growth disability when an ultrasound is conducted. Typically, people with primoridal dwarfism are born with very low birth weights. After birth, growth continues at a stunted rate, leaving individuals with primordial dwarfism perpetually years behind their peers in stature and in weight.

Most cases of short stature are caused by skeletal or endocrine disorders. The five subtypes of primordial dwarfism are the most severe forms of the 200 types of dwarfism, and it is estimated that there are only 100 individuals in the world with the disorder.[1] Other sources list the number of persons currently afflicted as high as 100 in North America.[citation needed]
It is rare for individuals affected by primordial dwarfism to live past the age of 30.[2] In the case of microcephalic osteodysplastic primordial dwarfism (MOPD) type II there can be increased risk of vascular problems, which may cause premature death.[3]
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Kesimpulan:
Dalam bahasa melayu kita panggil kes macam ni org kerdil la, tp macam artiekl tu bgtau, ada mcm2 jernis kekerdilan,kebantutan atau kekerdilan. Yang ni punya jenis, pembesaran stabil.. tak mcm yg biasa kita tgok..tula bila tgok org2 istimewa mcm ni, mmg rasa bersyukur sgt dgn diri sendiri walau kdgkala rasa x..huhu
wallahualam.
p/s: terimalah diri anda dan sayangilah diri anda seadanya, dan sayangi anak2 anda(bila aku nk dapat ank ni?huhu)

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