List Of Diseases Starting With M: Information From Answers.com Microcephalic osteodysplastic primordial dwarfism Microcephaly, holoprosencephaly,and intrauterine growth retardation; Microcephaly, primary autosomal http://www.answers.com/topic/list-of-diseases-starting-with-m
Extractions: showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Or search: - The Web - Images - News - Blogs - Shopping List of diseases starting with M Wikipedia List of diseases starting with M A list of diseases in the English wikipedia. A B C D ... L M N O P Q ... Z Macular corneal dystrophy Macular degeneration juvenile Macular degeneration, age-related
List Of Diseases Starting With I: Information From Answers.com Ichthyosis mental retardation dwarfism renal impairment; Ichthyosis microphthalmos intrauterine growth retardation mandibular malar hypoplasia http://www.answers.com/topic/list-of-diseases-starting-with-i
Extractions: showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Or search: - The Web - Images - News - Blogs - Shopping List of diseases starting with I Wikipedia List of diseases starting with I A list of diseases in the English wikipedia. A B C D ... H I J K L M ... Z Ichthyophobia Ichthyosiform erythroderma corneal involvement deafness Ichthyosis alopecia eclabion ectropion mental retardation Ichthyosis and male hypogonadism Ichthyosis bullosa of Siemens Ichthyosis cheek eyebrow syndrome Ichthyosis congenita biliary atresia Ichthyosis deafness mental retardation skeletal anomaly Ichthyosis follicularis atrichia photophobia syndrome Ichthyosis hepatosplenomegaly cerebellar degeneration Ichthyosis hystrix, Curth Macklin type Ichthyosis linearis circumflexa Ichthyosis male hypogonadism Ichthyosis mental retardation Devriendt type Ichthyosis mental retardation dwarfism renal impairment Ichthyosis microphthalmos Ichthyosis tapered fingers midline groove up Ichthyosis vulgaris Ichthyosis, erythrokeratolysis hemalis
ICD-9-CM From Code 250 259.4 dwarfism, not elsewhere classified. dwarfism. NOS; constitutional.Excludes dwarfism. achondroplastic (756.4); intrauterine (759.7) http://www.dmi.columbia.edu/hripcsak/icd9/1tabular250.html
Accessing Article Seckel syndrome (OMIM 210600) is an autosomal recessive disorder characterizedby intrauterine growth retardation, dwarfism, microcephaly and mental http://www.nature.com/ng/journal/v33/n4/full/ng1129.html
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Clinical Dysmorphology - UserLogin intrauterine growth retardation, a universal finding in the MOPD II, Osteodysplastic primordial dwarfism type II (MajewskiRanke type) with normal http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200210000-00005.htm
Clinical Dysmorphology - UserLogin primordial dwarfism type 2 is also characterized by intrauterine and postnatal Seckel dwarfism based on a personel case. Klin Padiatr 201134141. http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200401000-00017.htm
Free Online ICD9/ICD9CM Codes And Medical Dictionary dwarfism. achondroplastic (756.4). intrauterine (759.7). nutritional (263.2).pituitary (253.3). renal (588.0). progeria (259.8) http://icd9cm.chrisendres.com/index.php?action=search&srchtext=259.4
THE MERCK MANUAL, Sec. 19, Ch. 261, Congenital Anomalies All are characterized by dwarfism (usually with a normalsized trunk but with Transverse or longitudinal limb deficiencies due to primary intrauterine http://www.merck.com/mrkshared/mmanual/section19/chapter261/261g.jsp
HGF - Growth Disorders What is intrauterine Growth Retardation ( IUGR )? Disproportionate shortstature, commonly referred to as dwarfism, can manifest itself as shortlimbed http://www.hgfound.org/disordersframe.html
Extractions: What Are Growth Disorders? There are many causes of growth failure in children. Some are constitutional, some are genetic, and some are the result of hormonal disorders. In some cases the growth disorder may be recognized at birth; in others, a parent may be concerned that the child is the shortest in the class, still wearing the same size clothing as last year, and growing less than two inches a year. In these cases, a thorough medical evaluation by a pediatric endocrinologist (or other growth specialist) is necessary to determine if there is a growth disorder affecting the child's development. What is Human Growth Hormone (HGH) Deficiency HGH deficiency may occur at any time during infancy or childhood, with the most obvious sign being a noticeable slowing of growth. The deficiency may be genetic is some families. Although these children may also possess signs of low blood sugar or obesity, they display average body proportions and (average intelligence. Through the use of injections of synthetic HGF over a period of several years, physicians can help these children deficient in HGH to achieve average height. . What is Cushing's Syndrome (Cortisol, Stress, Hormone Excess)?
Extractions: This is a 15 year old boy who is seen by his primary care physician for short stature and delayed sexual development. His past medical history is unremarkable except for asthma during early childhood, which has been well controlled. He is currently on no medications. He is an average student currently in the 9th grade and is the smallest in his class. He has been harassed by older classmates because of his size. His parents are concerned because Jim is becoming withdrawn and a "loner". PMH: Pregnancy and delivery were uncomplicated. Birth weight and length were 3.86 kg (8.5 pounds) and 51 cm (20"), respectively. His HC was 35 cm. His immunizations are current. Family History: His mother is 48 years old and in good health. Her height is 167 cm (50th %tile). Her menarche began at age 13.0 years. His father is 51 years old, also in good health. His height is 184.0 cm (75th %tile). His father's onset of puberty is not known but he was shaving regularly by age 15. There is one older male sibling age 18 who is in good health. His puberty began at age 11 years. There is no history of smoking, alcoholism, mental illness, drug abuse or learning problems in the family. Exam: VS T 37.1, P 110, R 32, BP 100/60. Ht. 158 cm (3rd %tile), Wt. 42.0 kg. (10th %tile). He is pale and anxious but cooperative. His HEENT exam is normal. His chest is clear. Heart regular, no murmurs. His pulses are symmetrical and equal. There are no masses or areas of tenderness in his abdomen. Genitalia: Normal circumcised phallus, SMR (Tanner) pubic hair stage 1, genital stage 2. His testes are firm, 2.5 cm in length and 4 ml in volume. His scrotum is reddened and stippled. The remainder of his physical exam is unremarkable.
Achondroplasia Dwarfism - Diseases And Conditions | FindYourHope.com FindYourHope.com FREE Achondroplasia dwarfism Newsletter threedimensionalultrasound and intrauterine three-dimensional helical computer tomography. http://www.findyourhope.com/Site/Achondroplasia Dwarfism/Type/Diseases And Condi
DBGET Result: OMIM 601215 MOLECULAR GENETICS Seckel syndrome (210600) is an autosomal recessive disordercharacterized by intrauterine growth retardation, dwarfism, microcephaly, http://www.genome.jp/dbget-bin/www_bget?omim 601215
Extractions: UCSD Musculoskeletal Radiology bonepit.com Pathology Index .1 NORMAL ROUTINE PLAIN FILM exclude. normal variant (.13) .12 SPECIAL TECHNIQUE, PROCEDURE, PROJECTION Digital radiographic techniques, tomography, MR, nuclear medicine .1211 Computed tomography .12111 Unenhanced .12112 Enhanced with intravenous drip or bolus .12113 Dynamic enhanced technique .12114 Delayed scanning following enhancement (e.g., for detection of liver lesions) .12115 Spiral scanning .12116 CT angiography .12117 Three-dimensional reconstruction .12118 High-resolution technique .12119 Other, including serial enhancement studies (e.g., for diagnosis of hemangioma) .1214 Magnetic resonance (MR) .12141 Morphologic magnetic resonance imaging .121411 Spin echo .121412 Gradient echo .121413 Inversion recovery .121414 Chemical shift imaging .121415 Specific resonance suppressed include: fat suppression, water suppression .121416 High-speed imaging include: echo planar .121417 Magnetization transfer .121419 Other .12142 MR angiography (morphological vascular imaging) .12143 Contrast-enhanced studies, trace studies
NSW Health - ICD-9-CM 240-279 259.4 dwarfism, not elsewhere classified dwarfism NOS constitutional Excludesdwarfism achondroplastic (756.4) intrauterine (759.7) nutritional (263.2) http://www.health.nsw.gov.au/public-health/icd/240-279.htm
Extractions: Excludes : endocrine and metabolic disturbances specific to the fetus and newborn (775.0-775.9) Note : All neoplasms, whether functionally active or not, are classified in Chapter 2. Codes in Chapter 3 (i.e., 242.8, 246.0, 251-253, 255-259) may be used to identify such functional activity associated with any neoplasm, or by ectopic endocrine tissue. Excludes : neonatal thyrotoxicosis (775.3) The following fifth-digit subclassification is for use with category 242:
Seckel Syndrome... to birth (intrauterine growth retardation) resulting in low birth weight. continue after birth (postnatal) resulting in short stature (dwarfism). http://www.angrynakedpat.com/wwwboard/messages66/335.htm
Extractions: Seckel Syndrome is an extremely rare inherited disorder characterized by growth delays prior to birth (intrauterine growth retardation) resulting in low birth weight. Growth delays continue after birth (postnatal) resulting in short stature (dwarfism). Other symptoms and physical features associated with Seckel Syndrome include an abnormally small head (microcephaly); varying degrees of mental retardation; and/or unusual characteristic facial features including "beak-like" protrusion of the nose. Other facial features may include abnormally large eyes, a narrow face, malformed ears, and/or an unusually small jaw (micrognathia). In addition, some affected infants may exhibit permanent fixation of the fifth fingers in a bent position (clinodactyly), malformation (dysplasia) of the hips, dislocation of a bone in the forearm (radial dislocation), and/or other physical abnormalities. Seckel Syndrome is thought to be inherited as an autosomal recessive genetic trait.
Complete List Of MeSH-C Terms Found In References Related To list of MeSHC terms found in references related to intrauterine growthretardation, Salivary Gland Diseases 3 dwarfism 3 Lymphoma, B-Cell 3 http://www.bork.embl-heidelberg.de/g2d/list_mesh_disease.pl?U64589:Intrauterine_
The MAGIC Foundation intrauterine growth retardation may result from maternal infections, Skeletal causes, such as short limbed dwarfism, result from abnormal production of http://www.magicfoundation.org/www/docs/150
Extractions: Note: If you have difficulty understanding terms in this (or any other document) please refer to the More Information- section (lower left table) for Dictionary terms. If we have missed some terms, which you would find helpful in the dictionary, please let us know and we will add a definition for them. Thank you. It is often said that maintaining a normal growth pattern is nature's lab test for good health. Growth is influenced by many factors such as heredity, genetic or congenital, illness and medications, nutrition, hormones, and psychosocial environment. Measurements of growth-height and weight - are a very inexpensive service that should be offered by all health care providers rendering care to children. Additionally it is also important that these be done correctly and included as a part of sick visits as well as "well child" check-ups. Normal height growth rates vary according to age. Children during the first year of life should grow 7-10 inches. During the second year growth slows to an average of 5 inches /year. During the third year growth averages 3 inches/year. From age 4 years until puberty, growth should be at least 2 inches/year. Pubertal changes prompt a growth spurt of 2 ½ -4 ½ inches/year for girls usually starting by 10 years. However, boys experience both puberty and this growth spurt later - usually starting by 12 years and averaging 3 - 5 inches/year. After pubertal changes are completed and bone ends fuse, no further growth is possible.
Silver-Russells Syndrom - Små Och Mindre Kända Handikappgrupper Russell A. A syndrome of intrauterine dwarfism recognizable at birth withcraniofacial dysostosis, disproportionately short arms and other anomalities. http://www.sos.se/smkh/2001-29-128/2001-29-128.HTM
Extractions: HTML-version 1.0 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. Orsak till sjukdomen/skadan Symtom Dessutom styrks diagnosen ytterligare om barnet har: 5. Krokiga lillfingrar. Praktiska tips Resurspersoner kerstin.albertsson-wikland@pediat.gu.se
