A number of other eponyms, such as menkes steely hair disease, menkes kinky hair disease, trichopoliodystrophy, and menkes syndrome, have been used in scientific nomenclature. The disease affects development, both mental and physical. Additional signs and symptoms include weak muscle tone hypotonia, sagging facial features, seizures, developmental. Thoughmostpatients 9095% have a severe clinical course table 1, various forms ofthe. Feb 01, 2009 the neurologist who discovered maple syrup urine disease and xlinked kinky hair disease menkes disease, john menkes, m. In the 52 years since the original description of menkes kinky hair disease mkhd, advances in understanding the clinical, biochemical, and molecular aspects of this rare disorder of copper metabolism have outstripped progress in the design of effective therapies. The abnormality is a defect of transmembrane transport of copper resulting in increased copper deposition in intestine and pancreas, with copper deficiency in. The estimated prevalence of the disease is 1 in 100,0001 in 250,000.
These patients can present with failure to thrive, severe psychomotor retardation, seizures and hypopigmented hair, which is characteristic of this condition. The characteristics facies, fair complexion, chubby cheeks, sparse twisted fuzzy depigmented hair are all present in our case. Characteristic findings include kinky hair, growth failure, and nervous system deterioration. It results in low copper levels and subsequently, deficiency in copperdependent mitochondrial enzymes. Figure 2 imaging a magnetic resonance angiography reveals highly tortuous arteries of the brain. These cuproenzymes catalyze a diverse range of essential biochemical reactions. Symptoms of md usually appear within the first few months of life and include sparse, kinky hair. Epilepsy is one of the main clinical features of this disease but it has been described in detail by only a few authors. Aka kinky hair syndrome, it is the impaired ability to metabolize copper. Menkes steely hair syndrome definition of menkes steely.
Menkes chief contribution to medicine was his discovery of kinky hair syndrome or menkes disease. Menkes kinky hair disease request pdf researchgate. Menkes disease is caused by a defect in the atp7a gene. Menkes disease md, also known as menkes kinky hair disease, is a fatal neurodegenerative disease caused by a defect in copper metabolism. Clinical manifestations include failure to thrive, mental retardation, seizures, and characteristic hypopigmented kinky hair. Kinky hair disease proved a designation useful in detection of new cases, since the hair change is an easily remembered feature by which physicians can be alerted to the condition obrien, 1968. Media in category menkes disease the following 8 files are in this category, out of 8 total. The cdna has been recently sequenced and is known to code for a protein of. Menkes described a previously unrecognized entity of cerebellar and focal cerebral degeneration, with kinky hair, failure to thrive and early death occurring in boys only. Menkes syndrome is a disorder that affects copper levels in the body.
Menkes kinky hair disease choudhary sv, gadegone rw, koley s. Menkes kinky hair disease is a rare xlinked recessive disease nearly exclusively affecting males who present at 23 months of age due to abnormal functioning of copperdependent enzymes due to. A case report international journal of urology, vol. Dermatologic manifestations of menkes kinky hair disease. Md is inherited as an xlinked recessive trait, and as expected the vast majority of patients are males. Jun 30, 2019 subclass of, hair disease, metal metabolism disorder. Menkes disease definition menkes disease is a disorder affecting the bodys copper levels and characterized by sparse and coarse hair, growth and development problems, as well as deterioration of the nervous system.
Menkes disease is a lethal multisystemic disorder of copper metabolism characterized by connective tissue abnormalities, progressive neurodegeneration and peculiar kinky hair. The mottled gene is the mouse homologue of the menkes disease gene. Mar 30, 2020 menkes disease is a disorder that affects copper levels in the body. Nov 04, 2009 menkes disease md is a lethal multisystemic disorder of copper metabolism. Spontaneous retroperitoneal hemorrhage in menkes disease. Menkes disease an xlinked recessive condition omim. Jun 11, 2016 two cases of menkes disease belonging to different families are reported in order to illustrate different types of central nervous system involvement. We report two cases of menkes kinky hair disease in which mr and mr angiography were performed. Md primarily affects the nervous system and connective tissue with symptoms that tend to get worse over time. Features include unusual kinky hair, growth retardation, bony abnormalities, profound neurodevelopmental delays, and seizures.
Neuroimaging changes in menkes disease, part 1 american. Menkes disease, also known as trichopoliodystrophy or kinky hair kinky vessel syndrome, is an xlinked recessive disorder that results in a derangement in copper handling. Menkes kinky hair disease trichopoliodystrophy, steelyhair disease is an xlinked neurodegenerative disorder that occurs predominantly in males. Localisationofthemenkeslocus menkesdisease wasrecognisedto segregate as an xlinked recessive trait when it was first described in 1962 by menkes et al.
Menkes disease mnk, also known as menkes syndrome, is an xlinked recessive disorder caused by mutations in genes coding for the coppertransport. This report notes important changes in the eyes which were found on histological examination. His hair is depigmented and lusterless with pili torti and the skin is pale with eczema. May 31, 2019 subclass of, hair disease, metal metabolism disorder. Menkes kinky hair disease menkes kinky hair disease ahlgren, p vestermark, s. Menkes and colleagues described menkes disease in 1962 that reported five male infants in a family affected with a distinctive syndrome of neurologic degeneration, peculiar hair, and failure to thrive. In 1962, menkes encountered a male infant who, while developmentally normal at birth, quickly developed floppy muscle tone, seizures, and coarse, brittle hair. Three unrelated cases of menkess syndrome are described. Natural cure for menkes disease and alternative treatments. Like all xlinked recessive conditions, menkes disease is. Menkes disease is a rare multisystem xlinked disorder of copper metabolism. Flared metaphyses of the ulna and radius in a 5monthold patient with classic menkes disease. Menkes kinky hair disease is a rare xlinked recessive disease nearly exclusively affecting males who present at 23 months of age due to abnormal functioning of copperdependent enzymes due to deficiency of copper. The defect makes it hard for the body to properly distribute transport copper throughout the body.
Subclass of, hair disease, metal metabolism disorder. Introduction menkes disease is an xlinked recessive disorder of copper transport, leading to dysfunction of copperdependent enzymes. Menkes disease md is a lethal multisystemic disorder of copper metabolism. Neuroimaging in menkes disease ahmed mi, hussain n j. Menkes kinky hair syndrome is an xlinked recessive multisystemic lethal disorder of copper metabolism.
Some additional signs and symptoms may include weak muscle tone hypotonia, sagging facial features, seizures, developmental delay, and intellectual disability. Progressive neurodegeneration and connective tissue disturbances, together with the peculiar kinky hair are the main manifestations. Menkes kinkyhair disease trichopoliodystrophy, steelyhair disease is an xlinked neurodegenerative disorder that occurs predominantly in males. Jun 28, 2019 pathogenic variants lead to severe copper deficiency. Diverticula of the bladder in a boy with menkes disease. Menkes disease md is an inherited condition that impacts the way the body. Menkes disease md is a rare infantileonset neurodegenerative disorder caused by mutations in the xlinked atp7a gene. In menkes kinky hair disease, intestinal copper uptake is normal, but. Request pdf on sep 1, 2012, sanjiv v choudhary and others published menkes kinky hair disease find, read and cite all the research you need on researchgate. Their patients were five boys, representing two generations of one family, all of whom exhibited. Menkes disease genetic and rare diseases information center.
B t1 and c t2 mri sequences demonstrate generalized neuroatrophy and delayed myelination. The neurologist who discovered maple syrup urine disease and xlinked kinky hair disease menkes disease, john menkes, m. Menkes kinky hair disease associated with a large bladder diverticulum. Menkes disease md, also known as kinky hair disease, is a multifocal, degenerative disease of gray matter first described in 1962 by menkes et al. The disease is caused by an underlying defect of copper metabolism.
Cell culture studies in phenotypically normal female menkes carriers indicated that the menkes disease gene mnk was subject to random xinactivation, also supporting an x linked. Menkes disease genetic and rare diseases information. The menkes disease is also called kinky or steely hair disease. Mr demonstrated characteristic cerebrovascular tortuousity and thus may be a valuable aid in diagnosis and followup. Google scholar levinson b, vulpe c, elder b, martin c, verley f, packman s, gitschier j. The symptoms involve multiple organ systems, such as the brain, lung, gastrointestinal tract, urinary tract, connective tissue, and skin. The characteristic clinical features are steely hair, profound retardation, spastic quadriparesis, seizures, and hypothermia. Menkes disease mnk, also known as menkes syndrome, is an xlinked recessive disorder caused by mutations in genes coding for the coppertransport protein atp7a, leading to copper deficiency. Ppt menkes disease powerpoint presentation free to. Menkes disease or kinky hair syndrome is a multisystemic disorder with an x linked inheritance, and mutation of the gene atp7a located on xq. Menkes kinky hair disease, neuroradiology 00283940 10. The history of john hans menkes and kinky hair syndrome.
Postmortem examination revealed lesions of the elastic membranes of large and. Here, we describe a completely workedup case of a 4monthold male infant with very typical history and radiological features confirmed by biochemical and trichoanalysis. Menkes kinky hair disease is an xlinked recessive multisystem disorder caused by disturbances of copper metabolism due to mutation of patpase7 gene. In menkes kinky hair disease, intestinal copper uptake is normal, but copper transport to other tissues is affected. Menkes kinky hair disease choudhary sv, gadegone rw, koley. The affected infant may also appear to have a yellow appearance jaundice which is caused by excessive bilirubin in the blood hyperbilirubinemia.
Patients usually exhibit a severe clinical course, with death in early childhood, but variable forms exist and occipital horn syndrome ohs is the mildest form. Menkes kinky hair disease is a rare xlinked recessive disorder of copper metabolism. Menkes disease is an inherited disorder in which the body has a problem absorbing copper. Clinical expression of menkes disease in females with. A ten minute documentary on menkes disease a rare fatal genetic disorder. Menkes disease md is a rare infantile onset neurodegenerative disorder due to mutations in the x linked atp7a gene. Females are carriers of menkes syndrome, and their sons who have the gene have the disease. Horizontal eyebrows, pudgy cheeks, and cupids bow of the upper lip from the classical facies. Menkes disease nord national organization for rare. Menkes kinky hair disease is an xlinked recessive trait caused by mutations in the atp7a gene leading to disturbed copper metabolism contributing to low serum copper and ceruplasmin.
Menkes disease md is a rare xlinked recessive fatal neurodegenerative disorder caused by mutations in the atp7a gene, and most patients are males. Progressive neurodegeneration and connective tissue disturbances, together with the peculiar kinky hair are the. The clinical phenotype is marked by fine silvery wiry hair, doughy skin, connective tissue disturbances, and progressive neurologic deterioration. Menkes kinky hair syndrome medicosis perfectionalis. An early researcher of maple syrup urine disease as an intern at boston childrens. Menkes disease results in developmental delay, seizures, hypotonia which is more in trunkal muscle and feeding difficulties. A sexlinked metabolic defect in copper metabolism, characterized by sparse, brittle, twisted hair, failure to thrive, lack of muscle tone, seizures, and progressive deterioration of the brain. The gene for khd is about 200 kb in size and is located on the long arm of x chromosome xql3. Changes in the metaphyses of the long bones and tortuosity of cerebral arteries have been described.
Vestermark neuroradiological and pediatric departments, glostrup hospital, faculty of medicine university of copenhagen glostrup denmark summary four new cases of menkes kinky hair disease are reported with special attention to the vascular and particularly the. In the first case which documents the sexlinked recessive inheritance, arteriographic studies have shown that the vascularization of the brain was severely impaired. Progressive neurodegeneration and connective tissue disturbances, together with. Kinky hair disease khd was first described by menkes et al. Female carriers are mosaics of wildtype and mutant cells due to the random x inactivation, and they are rarely affected. Menkes disease md is an xlinked multisystemic lethal disorder of copper metabolism. The most promising therapy to date, very early subcutaneous copper injections, has normalized neurodevelopmental. It is characterized by brittle, tangled, sparse, steely or kinky hairs that are often white, ivory, or gray in color with easy pluckability. Sir, menkes kinky hair disease is a rare xlinked recessive disorder of copper metabolism. Roberts from the departments of paediatrics and histopathology, united norwich hospitals, norwich wheeler, e.
Menkes disease is characterized by dry skin and abnormal hair that is often brittle, tangled, sparse, steely or kinky and is often white, ivory, or grey in color. This gene encodes a coppertransporting atpase, which has the dual role of atpdriven copper efflux from cells and the intracellular transport of copper to the copperrequiring enzymes. Three unrelated cases of menkes s syndrome are described. Figure 1 characteristics of scalp hair in menkes disease hair is sparse, short, thin, fragile, and lightcolored, and has a steelwool appearance. Menkes, in rosenbergs molecular and genetic basis of neurological and psychiatric disease fifth edition, 2015. Progressive neurodegeneration and connective tissue disturbances, together with the peculiar kinky hair are the main. Using sequences from exon 10 fused to a nongolgi reporter molecule, francis et al. Despite an early, severe, and progressive neurologic involvement, our knowledge of brain involvement remains unsatisfactory. In the largest cohort of md patients reported so far which consists of 517 families we identified 9 neurologically affected. Their patients were five boys, representing two generations of one family, all of whom exhibited severe and early.
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