British girl has rare pygmyism is called the thumb girl

British girl fee silk · was Finn with rare dwarf,, 7 years old, weight equivalent to only a year and a half the normal development of children.
Mother Judith · was Finn says fee silk is "the thumb girl", but "broad mind".
"Mini"
Fee silk and family lives in Newcastle, sister grace · Finn was nine cheap oakley sunglasses years old, and her sister hope · Finn was 6 years old.
Fee silk birth weight of normal, about 3.66 kg, three sisters in the heaviest. Judith said: "she was born, my husband and I never thought she flint what's wrong and she looks so perfect... hope to 1 year old and fee long, others think silk they are twins."
Now, with the hope that the photo, fee only to sister silk height nba jerseys central upper arm, always let strangers think age difference between the two sisters. The three sisters collective go out, others to always take the fee silk as the smallest one.
In fact, the weight equivalent to wire now for a year and a half the normal development of children, wear school uniform is three years old children according to size is made.
seek
From the three months when starts, fee silk become extremely easy ill, often cough, and pulmonary infection. 11 months, fee silk sudden asthma symptoms, doctor check found that her water lung, heart ale defects.
Judith said: "she is just a few months old, will become the body is very poor, always a infection and then another. She was only 5 kg weight."
"The doctor originally thought to be heart valve defect let her digestive system appear problem, made her slow growth," Judith said, and gave her to do the surgery, for 9 hours, with artificial valve replacement valve problem, "the operation is a success, but she is still not development".
"People often because she said her delicate and lovely shape, but her with 1-2 years old when nothing different."
Later, the couple was Finn with fee silk to Newcastle a genetic center inspection, found her normal hormone levels, all body development and related inspection showed negative. "Her case is rare, we seek for many years, and the doctor trying to find out what she of what went wrong, has been unable to give the answer," Judith said.
miracle
Four years later, the doctor diagnosed fee silk with "smiling face type of bone stunted growth", is a dwarf. Fortunately, different from the part of the dwarf patients, fee silk figure scale is normal.
Gnome disease caused by a gene mutation. Finnan had was the incidence of dwarf for 200 million, only 30 patients around the world, for the performance of the very small and bone and joint, heart and skin abnormalities, some patients with liver get big. Patients can survive to adulthood.
Judith said: "we near collapse. We've never heard of this illness...... she really unfortunate."
After diagnosis, fee silk and receive two heart surgery, recent breathing difficulties and because the hospital.
In her daily life in meeting the inconvenience. After school, the university had in the classroom for her special steps; For lunch, she needs help cushion to come to the table.
Judith says fee silk is "mini miracle". She said, daughter small size, but have a "broad and heart", "her lively to the disease, not fear, joking around, said to the princess as she grew up..." little "people like to do, I don't want to grow up. Concentrated is essence, it was just the said fee silk".
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