http://www.articlealley.com en-us editorial@articlealley.com Applying fake eyelashes is best left to your makeup artist, but with a little patience and practice, you too can master this art. So don't attempt it 5 minutes before leaving to a huge party. Andrea lashes are big and they are available cheaply at the dru... http://www.articlealley.com/http://julietcohen.articlealley.com/how-to-apply-fake-eyelashes-1604745.html 17th June 2010 Maffucci syndrome is a really rare disorder. Maffucci syndrome is a disorder which affects the skin and skeleton, causing benign cartilage tumors, bone deformities, and dark hemangiomas to grow. Maffucci syndrome is characterized by benign overgrowths of ... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-maffucci-syndrome-668710.html 17th October 2008 Neurosyphilis is a gradually progressive and destructive infection of the brain or spinal cord. It is considered a life-threatening complication of syphilis. It occurs in untreated syphilis many years after the primary infection. This can lead to destruct... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-neurosyphilis-668687.html 17th October 2008 Muenke Syndrome, also known as FGFR3-related craniosynostosis. Muenke syndrome is an inherited condition characterized by the early closure of certain bones of the skull (coronal synostosis), which affects the shape of the head and face. Many people with ... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-muenke-syndrome-668049.html 17th October 2008 Marinesco-Sjögren syndrome is a unusual autosomal recessive disorder characterized by cerebellar atrophy, ataxia, cataracts, short stature and varying degrees of mental retardation. Marinesco-Sjogren syndrome can be related with mutations of the SIL1 gen... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-marinescosjogren-syndrome-668005.html 17th October 2008 Megalencephaly is a type of cephalic disorder and also called macrencephaly. Megalencephaly is marked by an abnormally large, heavy, usually malfunctioning brain. The head may be enlarged at birth or become abnormally big in the early years. The brain wei... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-megalencephaly-667995.html 17th October 2008 Melkersson-Rosenthal syndrome is a neurological disorder characterized by facial swelling, exceptionally of the lips. It involves nerves, mucous membranes, and skin, especially in orofacial region. Melkersson-Rosenthal syndrome is characterized by oral no... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-melkerssonrosenthal-syndrome-667946.html 17th October 2008 Microvillous inclusion disease is a rare inherited disorder of the small intestine that is inherited in an autosomal recessive pattern. It is caused by a congenital lack of apical microvilli in the epithelial cells of the small intestine. Microscopic pol... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-microscopic-polyangiitis-667834.html 17th October 2008 Meige's syndrome is a type of dystonia. Dystonia is a group of movement disorders that vary in their symptoms, causes, progression, and treatments. This group of neurological conditions is generally characterized by involuntary muscle contractions that fo... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-meige-syndrome-667791.html 17th October 2008 Monilethrix is an autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded. Mutations in the person basic hair keratins hHb1 and hHb6 have recently been reported in this disease. These changes in the helix-encoding a... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-monilethrix-667773.html 17th October 2008 Marinesco-Sjogren syndrome (MSS) is a rare disorder that is genetic as an autosomal recessive genetic condition. The main accentuates of this disorder are a loss of muscle coordination as a effect of an affect on the cerebellum (cerebellar ataxia), cloudi... http://www.articlealley.com/http://julietcohen.articlealley.com/detailed-information-on-marinescosjogren-syndrome-mss-667658.html 17th October 2008 Lymphomatoid papulosis (LyP) is a rare skin disorder. Lymphomatoid Papulosis is characterised by crops of self healing skin lesions that look cancerous under the microscope but are actually benign (non-malignant). Lesions contain unusual cells that are si... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-lymphomatoid-papulosis-650369.html 26th September 2008 Laron syndrome type I (LTD1) a rare genetic disorder. Laron syndrome is caused by the body's inability to use the growth hormone (GH) that it produces. Laron Syndrome is an uncommon genetic disease that causes humans to be short. Laron syndrome type I (LT... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-laron-syndrome-650088.html 26th September 2008 Lymphocytic colitis, a subtype of microscopic colitis. Lymphocytic colitis is a type of bowel inflammation that affects the colon (large intestine). The appearance of the inner colon lining in microscopic colitis is normal by visual inspection during colo... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-lymphocytic-colitis-648677.html 25th September 2008 Locked-in syndrome is also called is Cerebromedullospinal Disconnection. Locked-in syndrome is a rare neurological disorder characterized by complete paralysis of voluntary muscles in all parts of the body bar for those that manage eye movement. Locked-in... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-lockedin-syndrome-647809.html 24th September 2008 Kyrle disease is a rare pathologic condition due to a keratinization disturbance. Kyrle disease is characterized by the formation of large papules with central keratin plugs that may grow in a widespread distribution pattern. The illness is most closely c... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-kyrle-disease-647724.html 24th September 2008 Kleine-Levin syndrome is rare condition characterized by extreme require for sleep, food, and sexual disinhibition. Symptoms, which may last for days to weeks, include excessive food intake, irritability, disorientation, lack of energy, and hypersensitivi... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-kleine-levin-syndrome-647653.html 24th September 2008 Kearns-Sayre Syndrome belongs (in part) to a group of rare neuromuscular disorders known as mitochondrial encephalomyopathies. Kearns-Sayre Syndrome (KSS) is a very uncommon fatal multisystem disorder which generally affects female and males before the ag... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-kearns-sayre-syndrome-647327.html 24th September 2008 Kabuki syndrome is a condition primary noted in kids in Japan. Kabuki syndrome (KS), a inherited disorder characterized by odd facial features, skeletal abnormalities, and intellectual injury. In most cases, Kabuki syndrome arises spontaneously. Rarely, t... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-kabuki-syndrome-647292.html 24th September 2008 Scleroderma is a connective tissue disease involving skin, blood vessels and the immune system. In its systemic form, internal organ involvement can happen. Scleroderma is a fairly rare disorder in children. This rare disease affects approximately 5,000 t... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-juvenile-scleroderma-647271.html 24th September 2008 Jarcho Levin syndrome is a genetic birth defect which causes malformed bones in the spine (vertebrae) and ribs. The chest has a characteristic crab-like appearance. Childs born with Jarcho Levin syndromes have intricacy breathing due to their little, malf... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-jarcholevin-syndrome-647256.html 24th September 2008 Jackson-Weiss Syndrome (JWS) is a infrequent genetic disorder characterized by foot abnormalities. The feet show very broad big toes and webbing of the skin between the second and third toes. Additionally, the toes are angled inward. Bony foot defects app... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-jacksonweiss-syndrome-647221.html 24th September 2008 Intestinal pseudo-obstruction labels a rare group of diseases that may lead to failure of gut functions. Intestinal pseudoobstruction is the decreased ability of the intestines to push food through, and often causes dilation of different parts of the bowe... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-intestinal-pseudoobstruction-647202.html 24th September 2008 Infantile digital fibromatosis (IDF) is a benign asymptomatic nodular proliferation of fibrous tissue occurring almost exclusively on the dorsal and lateral aspects of the fingers or the toes. This lesion has also been referred to as Reye tumor, infantile... http://www.articlealley.com/http://julietcohen.articlealley.com/information-on-infantile-digital-fibromatosis-647129.html 24th September 2008 Greig cephalopolysyndactyly syndrome (GCPS) is a rare inherited disorder characterized by bodily abnormalities affecting the fingers and toes (digits) and the head and facial (craniofacial) area. The skin between the fingers and toes may be fused (cutaneo... http://www.articlealley.com/http://julietcohen.articlealley.com/greig-cephalopolysyndactyly-syndrome-631976.html 09th September 2008 Graft-versus-host disease (GVHD) is a common side effect of an allogeneic bone marrow or cord blood transplant (also called a BMT). An allogeneic transplant uses blood-forming cells donated by a family member, unrelated donor or cord blood unit. GVHD occu... http://www.articlealley.com/http://julietcohen.articlealley.com/graft-versus-host-disease-631953.html 09th September 2008 Good pasture syndrome also called anti-glomerular vault antibody disease. Good pasture syndrome is a disease that affects the kidneys and lungs. It is an autoimmune disease a condition in which the body's own security system reacts against several part of... http://www.articlealley.com/http://julietcohen.articlealley.com/good-pasture-syndrome-631946.html 09th September 2008 Grover's disease is characterized by an itchy eruption that may last an average of 10-12 months. Grover's disease frequently starts fairly suddenly. It is characterized by papules and papulovesicles with excoriations occurring on the chest, back, lower st... http://www.articlealley.com/http://julietcohen.articlealley.com/grovers-disease-631944.html 09th September 2008 Hemolytic Uremic Syndrome (HUS) is a serious disease that affects the kidneys and blood clotting system. Hemolytic-uremic syndrome is characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure. It is a rare ... http://www.articlealley.com/http://julietcohen.articlealley.com/hemolyticuremic-syndrome-631941.html 09th September 2008 Hemochromatosis is the most common form of iron overload disease. Hemochromatosis is characterized by excessive absorption of dietary iron resulting in a pathological increase in total body iron stores. The excess iron is stored in the body's tissues and ... http://www.articlealley.com/http://julietcohen.articlealley.com/hemochromatosis-631933.html 09th September 2008 Harlequin ichthyosis also known as Harlequin Type Ichthyosis. Harlequin ichthyosis is characterized by a thickening of the keratin layer in fetal human skin. Infants with this condition are born with very hard, thick skin covering most of their bodies. Th... http://www.articlealley.com/http://julietcohen.articlealley.com/harlequin-ichthyosis-631855.html 09th September 2008 Hantaviruses are a group of viruses found in wild rodents. Hantaviruses are a family of viruses that can lead to bleeding in the lungs and kidney damage. Prior to the outbreak in the southwestern United States, they were best known to cause disease from W... http://www.articlealley.com/http://julietcohen.articlealley.com/hantaviruses-631846.html 09th September 2008 Halo naevi, also known as leukoderma acquisitum centrifugum. Halo nevi are common benign skin lesions that represent melanocytic nevi in which an inflammatory infiltrate develops, resulting in a zone of depigmentation surrounding the nevus. They appear as... http://www.articlealley.com/http://julietcohen.articlealley.com/halo-naevi-631842.html 09th September 2008 Hairy tongue, also known as black tongue, is a gentle condition of elongation and staining of the fingerlike projections (papillae) on the tongue surface. This condition may be caused by overgrowth of a bacteria or yeast that produces a colored substance.... http://www.articlealley.com/http://julietcohen.articlealley.com/hairy-tongue-631838.html 09th September 2008 Hailey-Hailey disease is also known as familial benign chronic pemphigus. Hailey-Hailey disease is a rare disease of the skin. It can begin at any age, but it is most common in the late teenage years, twenties and thirties. Typically it appears as thin wa... http://www.articlealley.com/http://julietcohen.articlealley.com/haileyhailey-disease-631831.html 09th September 2008 Gigantomastia (also known as macromastia) is a condition in which a woman's breasts cultivate to too much size, usually as a consequence of pregnancy. The condition is caused by over-sensitivity to the woman hormones estrogen and progesterone, and/or an u... http://www.articlealley.com/http://julietcohen.articlealley.com/gigantomastia-detailed-information-631318.html 09th September 2008 Giant axonal neuropathy (GAN) is a degenerative disorder of the peripheral nerves that is inherited as an autosomal recessive attribute, presenting in early childhood and progressing to death, usually by late adolescence. Giant axonal neuropathy is caused... http://www.articlealley.com/http://julietcohen.articlealley.com/giant-axonal-neuropathy-gan-detailed-information-631283.html 09th September 2008 Gianotti-Crosti syndrome (GCS) is a different contagious exanthem with related lymphadenopathy and acute anicteric hepatitis. Gianotti-Crosti Syndrome is a rare skin disease affecting children between the ages of nine months and nine years. More than 90% ... http://www.articlealley.com/http://julietcohen.articlealley.com/gianotticrosti-syndrome-detailed-information-631280.html 09th September 2008 Galactokinase deficiency, also known as Galactosemia type 2 or GALK deficiency. Galactokinase deficiency (GKD) is an inherited disorder of galactose metabolism. It is characterized by galactosuria and galactosemia that is caused by a deficiency of the gal... http://www.articlealley.com/http://julietcohen.articlealley.com/galactokinase-deficiency-detailed-information-631223.html 09th September 2008 Fucosidosis is inherited as an autosomal recessive genetic trait. Fucosidosis is a really uncommon hereditary lysosomal storage disease characterized by a deficiency of the enzyme alpha-L-fucosidase. This disorder belongs to a group of diseases known as l... http://www.articlealley.com/http://julietcohen.articlealley.com/fucosidosis-types-1-detailed-information-631172.html 09th September 2008 Fox-Fordyce disease is an rarely happing chronic pruritic papular eruption that place to areas where apocrine glands are create. This condition is also referred to as ‘apocrine duct occlusion' and ‘sweat retention disease'. Fox-Fordyce disease is most... http://www.articlealley.com/http://julietcohen.articlealley.com/foxfordyce-disease-detailed-information-631129.html 09th September 2008 Fissured tongue, also called scrotal tongue. Fissured tongue is a benign condition characterized by deep grooves (fissures) in the dorsum of the tongue. The surface furrows may differ in size and depth, radiate outward, and cause the tongue to have a wrin... http://www.articlealley.com/http://julietcohen.articlealley.com/fissured-tongue-detailed-information-631121.html 09th September 2008 Ablepharon macrostomia syndrome is an exceedingly uncommon inherited hereditary disorder. The precise reason of Ablepharon macrostomia syndrome is not amply understood, some cases indicate that the disorder may be inherited as an autosomal recessive hered... http://www.articlealley.com/http://julietcohen.articlealley.com/complete-information-on-ablepharon-macrostomia-syndrome-with-treatment-and-prevention-563453.html 25th June 2008 Cretinism is a circumstance of seriously stunted physiological and psychological increase payable to raw inborn inadequacy of thyroid hormones. Cretins have dwarfed bodies, with curvature of the backbone and pendulous stomach. Their limbs are distorted, t... http://www.articlealley.com/http://julietcohen.articlealley.com/complete-information-on-cretinism-563133.html 25th June 2008 Cutis laxa too called elastolysis. It is a group of uncommon connective tissue disorders in which the rind becomes inelastic and hangs broadly in folds. Cutis laxa can be balmy, affecting simply an individual's show, or serious, affecting the domestic org... http://www.articlealley.com/http://julietcohen.articlealley.com/complete-information-on-cutis-laxa-563117.html 25th June 2008