Prenatal testing for ichthyosis Expand Ichthyosis is normally caused by changes in the genes we inherit from our parents, but can also develop later in life. These changes in our genes are known as mutations (also known as variants), and they change the way that the skin develops and lead to excess of skin growth. We know many of the changes in our genes which lead to the various types of ichthyosis and this allows us to diagnose the condition early on. Inheritance patterns in ichthyosis can be either dominant, recessive or X-linked. This means that depending on the type of ichthyosis you have, there are different percentage chances that the condition will be inherited. What is Prenatal Testing? Prenatal testing is a method that can be used during pregnancy to identify if the unborn baby has ichthyosis. If parents have a child with ichthyosis, genetic testing is performed to find out which gene variant has caused the ichthyosis. Prenatal testing can then be used to identify if the unborn child has the variant which causes ichthyosis in this family. Types of Prenatal Testing Chorionic Villus Sampling (CVS): 11-13 weeks. In CVS a needle is used to take a piece of the placenta, which has the same genetic information as the unborn baby. This placenta is then tested to see if the genetic variant causing ichthyosis is present. Amniocentesis: 15-18 weeks. In Amniocentesis a needle is used to take a small amount of amniotic fluid, which has some of the unborn baby’s genetic material. This fluid can then be tested to see if the unborn baby has the gene variant causing ichthyosis. Non-Invasive Prenatal Diagnosis (NIPD): NIPD is a blood test which can examine foetal DNA in the mother's blood. A special assay has to be developed. This has been developed in the NHS for some rare inherited disorders eg cystic fibrosis and some forms of muscular dystrophy, but is not yet available for ichthyosis. Pre-implantation Genetic Diagnosis (now also known as preimplantation genetic testing for monogenic disorders [PGT-M]): This method involves in vitro fertilisation (IVF). Eggs from mother and sperm from father are combined in the laboratory and then embryos can be tested for the gene variant causing ichthyosis and only embryos without the variant are implanted into the womb. Considerations Benefits: Early Detection: Prenatal testing allows you to test and thus identify ichthyosis early. This can help you make informed decisions about pregnancy. Preparation: It may be helpful for you to know what to expect before your child is born. Ichthyosis is associated with challenges and preparing yourself can help face these. Challenges: Procedural Complication Risks: CVS and amniocentesis are both invasive tests, and there is a small risk of miscarriage or complications such as infection and damage from the needle Treatment Options: While prenatal testing can provide early diagnosis, treatment options for ichthyosis are often focused on managing symptoms rather than a cure. Funding: Prenatal testing will require a consultation with a clinical geneticist and a genetics counsellor and then approval for prenatal testing. Factors to Consider when making a decision: Information: Make sure you have gathered information on ichthyosis including the types which can be tested for and the treatment options available. Remember there may be new treatments on the horizon. Also make sure you have sought information on the prenatal testing process where you live, including waiting lists and funding, and what your options are after testing. Currently approved by Human Fertilisation & Embryology Authority: Ichthyosis (X-linked, XLI), Harlequin ichthyosis, Ichthyosis follicularis-alopecia-photophobia Syndrome; IFAP Syndrome 1 With or Without Bresheck Syndrome; (IFAP1), Ichthyosis with confetti, Ichthyosis, cyclic, with epidermolytic hyperkeratosis (ICEHK), Ichythosis hystrix of Curth-Macklin. Professional Consultations: A consultation with a genetic counsellor can be a useful source of further information. Here you can discuss benefits and risks of prenatal diagnosis, and ask any questions you might have. Personal: Prenatal diagnosis is a personal decision which depends on your values, beliefs and personal choice! It can be helpful to involve family and friends for support, but remember the decision is yours. If you have a partner, make sure to discuss the options with them. Conclusion Decisions about Prenatal testing for ichthyosis are very personal and there are many things to consider. It can be helpful to discuss your options with people close to you, professionals or those with prior experience. Support groups can be a useful source of meeting people with experience and in similar situations. There is no right or wrong answer and it is important to understand the risks, benefits and possible outcomes when making a decision that aligns with your personal values and preferences. Please seek guidance from healthcare providers or genetic counsellors for further guidance. Charlotte is an aspiring Dermatologist who is currently undertaking an MRes in Human Tissue Repair at University College London and works as a doctor at University College London Hospital in London. She completed her undergraduate medical studies at University of Cambridge, Trinity College where she intercalated with a BA in Genetics. Dr Charlotte Muehlschlegel, University College London Hospital, MB BChir, BA, MA (Hons)
Inheritance of Ichthyosis Factsheet Expand Introduction There are many different types of ichthyosis. None of them are catching or contagious but they all depend on a small genetic mistake which has often been inherited from ones parents. There are 3 basic patterns of inheritance but a basic understanding of genetics is needed to understand how this occurs. We all have billions of genes. Each gene has a specific function such as to make a protein or fat within the body. Each gene is made up of tens thousands of building blocks called nucleotides. When these complicated genes replicate it is not uncommon for there to be very small mistakes. A single nucleotide (out of many thousands) may be changed or in the wrong position in the gene. Often this causes no problem or disease at all as the gene can still function. However if the mistake is in a crucial position in the gene – it may make the gene malfunction so that it can’t produce, for example, a skin protein, and this may lead to a disease such as ichthyosis. In practice most human beings have a number of small genetic mistakes and these do not cause disease. Only when these mistakes stop a gene from working normally does a disease arise. How do we inherit genes from our parents? Every human being has 2 copies of each gene. However the father’s sperm and the mother’s egg have only 1 copy of each gene. This means that when the egg and sperm join to make a new baby, the baby will have 2 copies of each gene just like its parents. So on average half your genes come from your mother and half from your father. An example of the blood group genes illustrates this: Mother gene AA - Father gene BB Mother’s egg gene A Father’s sperm gene B Sperm and egg join Baby gene AB Dominant and recessive genes As we have mentioned genes come in pairs. These may be identical genes (eg DD or dd) or non-identical genes eg (Dd). Let’s say that this gene causes hair colour. For example gene D may cause black hair and gene d blond hair. If gene D is said to be a dominant gene it will dominate over gene d. This means that anyone with the gene combination DD or Dd would have black hair. Only those individuals with gene combination dd would have blond hair. Therefore gene d is called a recessive gene. 2 copies of a recessive gene must be present before it can express itself. Example 1 Mother DD - Father dd black hair - blond hair Either gene can be passed on Egg can be only D - Sperm can only be d Possible combinations for child All children will be Dd All children will have black hair Example 2 Mother Dd - Father Dd Black hair - black hair Either gene can be passed on Egg can be D or d - Sperm can be D or d Possible combinations for child 25% DD - 50% Dd - 25% dd black hair - black hair - blond hair Autosomal dominant disease (eg ichthyosis vulgaris) Let’s take the above a step further to see how this fits with disease. Say gene h is a normal gene. Gene H is an abnormal gene with a small mistake that stops it from working normally. Example Disease gene H is dominant. All individuals with Hh or HH will have the disease. Individuals with hh will be normal. Mother Hh - Father hh (has disease) - (no disease) Either gene can be passed on Egg could be H or h - Sperm can only be h Possible combinations for child 50% Hh - 50% hh has disease - no disease This pattern of inheritance is called autosomal dominant. It means if one parent is affected there is a 50% chance of a child being affected. Autosomal recessive disease (eg lamellar ichthyosis) Example Disease gene H is recessive (Normal gene h is dominant) Only individuals with HH will have the disease. All individuals with hh or hH will be normal. However hH individuals will be carriers for the disease. Mother hH - Father hH (carrier) - (carrier) Either gene can be passed on Egg could be H or h - Sperm could be H or h Possible combinations for child 25% HH 50% Hh 25% hh have disease no disease no disease (is a carrier) This pattern of inheritance is called autosomal recessive. Neither parents are affected but both are carriers. On average 25% of their children will be affected, 25% normal and 50% will be unaffected carriers. So how do I know if I am a carrier for a recessive gene? You don’t because a carrier does not have the disease. In fact most people care carriers for a number of recessive genes. Let’s say you were a carrier for 5 different diseases. This is only 5 genes out of the many millions of genes that you have. If each individual only carries 5 abnormal recessive genes it is very very unlikely that your partner would have mistakes in the exact genes. It is therefore extremely unlucky when you have children with somebody who is a carrier for the same condition as this can produce a child with a disease. Marrying within your own family (eg a first cousin) increases your chances of your few abnormal genes being the same as your partners and thus increase the chances of producing autosomal recessive disease. Sex-linked recessive disease (also called X-linked disease) We have already mentioned that all humans carry 2 copies of their genes. There is one partial exception to this and this involves the sex genes (or sex determining genes). Females have 2 X-chromosomes which carry the sex genes. However, males only have 1 X-chromosome and 1 Y-chromosome. Therefore they do not have 2 copies of the X-chromosome genes. This is important if a male has an abnormal gene on the X-chromosome. Even if this gene is recessive he will have the disease as he doesn’t have a second copy to override this. Example (X-linked ichthyosis) Normal gene T is dominant Disease gene t is recessive Remember males only have 1 X-chromosome Mother genes Tt - Fathergene T + “absent second copy” no disease - no disease (carrier) Either gene can be passed on Egg could be T or t - Sperm is T or “absent second copy” Possible combinations for child 50% girls - 50% boys 25% TT - 25% Tt - 25% T - 25% no disease no disease no disease has disease (carrier) So for X-linked recessive conditions females are normal or carriers whereas males are normal or have the disease. This is why X-linked ichthyosis only occurs in males. Interestingly if an affected male has children none will be affected so it appears to “skip” a generation. In fact all his daughters are carriers and all his sons will be normal. X-linked dominant disease (eg Conradi-Hünermann syndrome) This is extremely rare. Here the abnormal gene on the X-chromosome dominates the normal copy. This causes disease in females and there is a 50% chance of passing this on to their daughters. This abnormal gene is so severe in males who have no second copy that it appears to be incompatible with life. Therefore X-linked dominant ichthyosis is not seen in males. Mothers genes TT - Father gene t + “absent second copy” no disease - has disease Either gene can be passed on Egg can be T only - Sperm is t or “absent second copy” Possible combinations for child 50% girls - 50% boys 50% Tt - 50% T no disease no disease (all carriers) So how do we apply this to ichthyosis? The first step is for your doctor to diagnose which type of ichthyosis you have. Once this is achieved he will explain how this condition is inherited. Autosomal dominant conditions Ichthyosis vulgaris Bullous ichthyosiform erythroderma KID syndrome Autosomal recessive Non-bullous ichthyosiform erythroderma Lamellar ichthyosis “Limited” lamellar ichthyosis Sjögren Larsson syndrome Netherton’s syndrome Harlequin ichthyosis Refsum’s disease Trichothiodystrophies (IDIDS syndrome) X-linked recessive X-linked ichthyosis X-linked dominant Conradi-Hünermann syndrome (also called X-linked dominant ichthyosis, Happle syndrome and chondrodyplasia punctata) Conditions can appear in a child when neither parent is affected. This is usually because the disease gene is newly created (new mutation) and may have occurred when the sperm or egg were produced. As the mistake is not present in the parents the risks of them having a further affected child are low. However the affected child has a chance of passing the condition on to their offspring when they are older depending on the affected gene. This sounds complicated but all this really means it that a genetic mistake has to start somewhere. Further help There are a number of online forums about Ichthyosis where individuals can share their experiences and detail their own treatment recommendations. Not everything will work for everyone but these forums are a good place both to receive and offer support. Contact the Ichthyosis Support Group for information, advice, details on useful products, and to be connected with other people to share experiences and helpful advice. Download The Inheritance of Ichthyosis Factsheet To find out more about the ISG or become a member please get in touch in one of the following ways: By Phone 0800 368 9621 By Email: [email protected] Facebook: facebook.com/ichthyosissupportgroup Twitter: twitter.com/ISG_Charity
Genetic Testing Expand Genetic testing Professor Celia Moss, Consultant Dermatologist, Birmingham Children’s Hospital (updated by Professor Edel O’Toole- 30.04.2014) Patients with ichthyosis, or their parents, naturally want as much information about their condition as possible. A common request is for “genetic testing”. But many people have a rather vague idea of what genetic testing means - not only patients, but also many doctors. This article will try to explain. What is a gene? Genes are the physical instructions, copied from one generation to the next, that programme us to be what we are. They consist of the chemical DNA. Identical sets are packed into the nucleus of every single cell in the body, arranged on chromosomes, like beads on a string. There is at least one gene, and sometimes hundreds, for every item of body structure and function. There are many genes responsible for the skin: these genes are present in all other organs as well as skin, but they are mostly “silent” in other organs, and only “expressed” in the skin. The “human gene map” has been published, so the names and locations of all human genes are now known. But scientists are still a long way from understanding what they all do, and research is going on all the time. How do genes cause disease? If there is a mistake (mutation) in the DNA of a gene, that gene may not work properly and can cause a genetic disease. For example, a mistake in the keratin 10 gene means that the structure of the epidermis is defective, causing epidermolytic ichthyosis, previously known as bullous ichthyosiform erythroderma (BIE). We have two copies of every gene, one from each parent. Some genetic diseases result from a mutation in only one copy of the gene (“dominant conditions” like BIE). Others only occur if there is a mutation in both copies (“recessive conditions” like congenital ichthyosiform erythroderma CIE). The parents of children with recessive conditions are usually “unaffected carriers” (mutation in just one copy). What genes cause ichthyosis? We know about several genes that can cause ichthyosis and the list gets steadily longer as more are discovered. For each gene, many different mutations have been recognised, perhaps explaining why the same condition can appear slightly different in different families. What is genetic testing? The term “genetic testing” covers all methods of investigating genes. It requires living cells, and the most convenient source of these is blood. Chromosomes are big enough to see under a microscope, using a technique called cytogenetics. But only very large mutations can be detected in this way. Most mutations can only be detected by chemical analysis of DNA which is usually extracted from blood cells. DNA can also be obtained from saliva but it is a bit less reliable - imagine if the smear picks up some germs, or a bit of meat from your dinner, it won’t be your DNA that gets tested! Usually saliva samples are obtained after rinsing out the mouth and before lunch, rather than after. Why does it take so long to get the results? Mutation testing is difficult and laborious. Many genes are large and complex, so it can be like looking for a needle in a haystack. Even if the lab finds an abnormality, it might not actually be the cause of the disease, because of “normal variation” (so-called polymorphisms): for example my normal keratin10 gene might not be exactly the same as someone else’s, even though it does the same job. So there can be “false negative” and “false positive” results. For some genes there are known “hot-spots” or short-cuts for finding common mutations. But even then the results must be thoroughly checked. When you finally get the result you can be confident that it is correct, and if you are still waiting for a result after many months or years it is usually because the lab hasn’t yet found a mutation. Is genetic testing used to make a diagnosis? No, usually it’s the other way round – we need to know the diagnosis to decide what gene or genes to test! However, now technology is available called exome sequencing and it is possible to test all known ichthyosis and skin disease-related genes quickly from one individual. However, there is a huge amount of information and a lot of expertise is required to perform analysis. At the moment, it is mainly performed in research labs and takes about 3 to 6 months. So how do doctors diagnose the type of ichthyosis? Doctors have a standard way of making a diagnosis. First we “take a history” asking questions about the way the ichthyosis developed (eg collodion baby), other cases in the family, and any other medical problems like deafness, eye problems or delayed development. Then we examine the patient and look at the pattern, severity and type of scales, whether there are blisters, and whether there are other physical abnormalities. Thirdly, depending on what we think it might be, we may request some laboratory tests, like a blood count, steroid sulphatase measurement, hair analysis, or occasionally skin biopsy. We might also request an opinion from another specialist (eg a neurologist or ophthalmologist) if there is an associated problem that might be relevant. After all that we can usually make a diagnosis. When is genetic testing carried out? A diagnosis of ichthyosis can be made without genetic testing. In recent years genetic testing has been mainly carried out for the purpose of genetic counselling, particularly in recessive conditions. If the causative mutation can be identified in a person with a recessive type of ichthyosis, then relatives can be tested to see if they are carriers, and unborn babies can also be tested (“prenatal diagnosis”). However, recent European and UK rare disease legislation will probably result in an attempt to give any patient, certainly with a severe ichthyosis, a genetic diagnosis. When is genetic testing not carried out? If we have absolutely no idea of the diagnosis, genetic testing is unlikely to help, because we don’t know which test to ask for. For example, genetic testing is not useful in a collodion baby initially because lots of genetic conditions can cause that appearance. With time the true diagnosis usually becomes apparent simply from observing the patient, and can be confirmed by genetic testing if necessary. For some conditions we don’t know the gene yet (eg some types of erythrokeratoderma), or there may be several candidate genes (like CIE), and it would be expensive and unrewarding to do tests. But even if there is no test at the current time, more genes are being found every year, and the situation can be revisited when the child is older. Sometimes parents ask for their unaffected children to be tested to see if they are carriers, but carrier testing is not carried out on children when the result has no relevance to them and they are too young to understand the implications. Who can request it? Genetic testing for ichthyosis is usually requested by a geneticist or dermatologist. In theory GP’s can request it, but usually they would not have the expertise to know what test to request, or how to interpret the result. Patients can request some genetic tests (“direct to consumer genetic testing”) but we would advise against this. Firstly, as with GPs, lay people do not have the breadth of knowledge required to request and interpret genetic tests. Secondly it costs hundreds and sometimes over a thousand pounds, which the NHS will pay for if it is requested by a health professional. Who does genetic testing? When a new gene is discovered, usually only the research lab that discovered it will test for it. While it is still new and interesting, labs will do the test for free (provided the request comes from a reliable dermatologist who is likely to have made the right diagnosis and requested the right test). Later they start to charge a commercial rate for the test, and subsequently big commercial labs will add that gene to their range on offer. Web sites offering genetic tests include www.ukgtn.org and www.genetests.org. Who gets the result? The result is sent to the person requesting the test. I usually send it on to the GP and the patient, with an explanatory letter, but very few doctors do that. I know that patients are unlikely to understand the report, but it seems to me to be a very important piece of information which rightly belongs to the patient. You can request a copy of the report from your doctor if you wish. DNA tests requested for medical purposes are confidential and never shown to any one other than the family and their medical professionals without the patient’s consent. What are the benefits of genetic testing? Having a genetic diagnosis is more precise than a clinical diagnosis, as you will know the exact mutation causing ichthyosis in your family. As explained above, a genetic diagnosis is necessary for prenatal diagnosis. Finally, it is likely that in the future (10-20 years) treatment may be based on the gene affected, so to be able to participate in trials of some new treatments, a genetic diagnosis may be needed. Any more questions? If you have further questions after reading this, you can email them to the ISG and we will try to answer them. Download The Genetic Testing Factsheet To find out more about the ISG or become a member please get in touch in one of the following ways: By Phone 0800 368 9621 By Email: [email protected] Facebook: facebook.com/ichthyosissupportgroup Twitter: twitter.com/ISG_Charity