Showing posts with label Cutis Laxa. Show all posts
Showing posts with label Cutis Laxa. Show all posts

Wednesday, January 28, 2015

ATP6V0A2 Gene …… Location

Cytogenetic Location: 12q24.31
Molecular Location: Base pairs 123,712,317 ~ 123,761,754 on chromosome 12




The ATP6V0A2 gene is located on the long (q) arm of chromosome 12 at position 24.31, precisely from the base pair 123,712,317 to base pair 123,761,754.


Tuesday, January 27, 2015

ATP6V0A2 Gene ... Official Name

Official Name: ‘ATPase, H+ transporting, lysosomal V0 subunit a2’

Official symbol: ATP6V0A2 

The ATP6V0A2 gene is also known by the following name:

E  A2V-ATPase
E  ATP6a2
E  ATP6N1D
E  J6B7
E  Stv1
E  TJ6
E  TJ6M
E  TJ6s
E  Vph1
E  VPP2_HUMAN



Wednesday, January 14, 2015

Genes…… (2/2)

Most of the genes are the elements of fibers ¾ slender bundle of protein provide strength and flexibility to connective tissue throughout the body. Elastic fibers allow the skin to stretch ¾ the lungs to expand & contract and arteries to handle the pressure of blood flow.

The major component of elastic fibers ¾ Elastin ¾ is produced from ELN gene. Other critical proteins of elastic fibers are produced by the following genes:

E EFEMP2
E FBLN5
E ATP6V0A2 

Mutations in any of these gene hamper the formation, assembly or function of elastic fibers.

Now, a shortfall in elastic fibers weakens connective tissue in the skin, arteries, lungs and other organs. These mutations in connective tissue cause the major feature of ‘Cutis Laxa’ to a small percentage. Researcher suspects that mutation in other genes, which is yet to identify may also be responsible for Cutis Laxa.


The chances of Acquired Cutis Laxa (ACL) are very rare. Acquired Cutis Laxa (ACL) is caused by the destruction of normal elastic fibers and not by inheritance. Though the causes of ACL are unclear, but it may occur due to the side effect any medical treatment which remove copper from body.




Tuesday, January 13, 2015

Genes…… (1/2)

Cutis Laxa is caused by the mutation in the following genes:

E ATP6V0A2
E ATP7A
E EFEMP2
E ELN/FBLN5


Wednesday, January 7, 2015

Inheritance .....

Most of the cases Cutis Laxa is inherited. There generally 3 types of forms of genetic inheritance…

E Sex Linked
E Autosomal Dominant
E Autosomal Recessive

The Autosomal Recessive form is the most common & severe.


Sex-linked
The defective/mutated gene is carried on one of the sex chromosomes, in this case it is located on the X chromosome
Autosomal Dominant
Only one copy of the defective/mutated gene is enough to cause CL. A child has a 50% chance of inheriting the gene from either parent.
Autosomal Recessive
In this type the affected child must inherit two copies of the defective/mutated gene from both of its parent. The chance of transmitting an autosomal recessive disease is 25% for each pregnancy.


Monday, January 5, 2015

History .....

Historically, Cutis Laxa (CL) was often confused with EDS (Ehlers Danlos syndrome), until 1923, when E. Parkes Weber noted the clinical differences between these two condition.


The internal involvement and the systemic nature of CL were elucidated by Goltz and co-workers, who emphasized the phenomenon of generalized elastolysis in same patient.


Thursday, November 27, 2014

Prevalence .....

The prevalence of ‘Cutis Laxa’ is estimated 1 in every 1,000,000 birth.


Cutis Laxa is extremely rare. As per National Institute of Health, only around 200 families are suffering from this disorder, worldwide.


Tuesday, November 25, 2014

The Name .....



The term ‘Cutis Laxa’ is a Latin word which means ‘Loose/Lax Skin


Wednesday, November 19, 2014

Cutis Laxa is all about ……

In a one liner Cutis Laxa is a rare inherited connective tissue disorder, characterized by inelastic saggy skin, with droopy appearance.


Connective tissue is the body’s supporting framework of tissue consisting of strands of collagen, elastic fibers between muscles and around muscle groups, blood vessels and simple cells. Connective tissue provides stricture and strength to the muscles, joints, organs and skin.


Tuesday, November 18, 2014

Meet the Little Yuxin ..... (2/2)

The little, Yuxin Xiaoli was born with a loosening skin. Her tiny face is full of wrinkles. The skin on her cheeks and chins drooped. She had even more sagging skin in other parts of her body.

Маленькая девочка выглядит как старушка

Przerażająca choroba! Ta "babcia" ma... 18 miesięcy

The little girl¿s face is covered with wrinkles, and the skin on her cheeks hangs. The skin on her body is even looser


Przerażająca choroba! Ta "babcia" ma... 18 miesięcy

Przerażająca choroba! Ta "babcia" ma... 18 miesięcy

Yuxin’s health is deteriorating ¾ she is suffering from a congenital heart disease, pneumonia and asthma, which recurring frequently these days.



Sunday, November 16, 2014

Meet the Little Yuxin ..... (1/2)

Meet Yuxin Xiaoli, a 3 year old girl in China ¾ but wait a minutes isn’t she looks like 60 ???

What Happened to her ??

Yuxin Xiaoli is thought be suffering from  cutis laxa, which is a group of rare connective tissue disorders in which the skin becomes inelastic and hangs loosely in folds.Yuxin Xiaoli is thought be suffering from  cutis laxa, which is a group of rare connective tissue disorders in which the skin becomes inelastic and hangs loosely in folds

Most of you are thinking that she might be suffering from a premature aging disorder ¾ Progeria??

Nope ----- not at all !!


It’s the rare skin disorder ¾ Cutis Laxa, which makes her look like an old woman.


Monday, November 10, 2014

Meet Zara ..... (2/3)

Zara and her sister Jolene and mum Tracy suffers from a rare disorder ¾ Cutis Laxa, though it was misdiagnosed as ‘Lipodystrophy’ earlier, which causes their skin appears saggy but not stretchy pointing to the premature aging.

lipodystropy family
 Tracey Gibson: 42, and two daughter Jolene Hardy: 24 and Zara Hartshorn: 16

Cutis Laxa is a rare genetic condition in which deterioration in the fatty and connective tissues as well as bones under the skin appears as the extreme premature aging. Some of them reported that their teeth fall out and have had to rely on collagen injection to combat wrinkles.



In contrast to 'Cutis Laxa', ‘Lipodystrophy’ is an extremely rare disorder in which fat deposited in the body parts, where it should not be allowed to deposit. With other health complication 'Lipodystrophy' makes a person look and appear older than his/her original age.



Wednesday, November 5, 2014

Meet Zara ..... (1/3)

Meet Zara Hartshorn, a British lady whose rare genetic condition has made her appear as 60, as if she is in the twilight of her life ¾ her teeth are falling out and she is on collagen injections for her wrinkles ¾  but Zara is no longer a middle aged woman who is coping to rejuvenate her youth ¾ she is only in her 16 !!!

Zara Hartshorn



Zara Hartshorn

Zara with her Birth Certificate

Zara Hartshorn


Thursday, October 30, 2014

Benjamin Button Disorder !!!

When I was a child I often put my feet in my dad’s shoe and start behaving like him ….. I always had a dread of commanding …… I always wished if I could grow up in the very next morning I would also be like my father …… I am sure many of us have this kind of thought at some point of time in childhood ……

But have you guys ever thought what if someone threats you as mom/granny when you are just in your sweet 16 ???

Found any resemblance with the move 'The Curious Case of Benjamin Button' played by Brad Pitt  ¾¾

You are right !!!

My next posts will be discussing on the Reverse Benjamin Button Disorder

Keep Reading J