*  atopic dermatitis

... and neonatal diseases and abnormalities hereditary congenital , inborn genetic diseases , genetic skin diseases , atopic ... The atopic diseases asthma, atopic dermatitis, and allergic rhinitis are the most common chronic diseases in children, and ... of human diseases, including inflammatory bowel disease, sexually transmitted and opportunistic infections, atopic dermatitis, ... of human diseases, including inflammatory bowel disease, sexually transmitted and opportunistic infections, atopic dermatitis, ...
https://labome.org/topics/diseases/and/inborn/genetic/atopic-dermatitis-8071.html

*  Craniosynostosis syndrome (Concept Id: C0010278) - MedGen - NCBI

A congenital disorder characterized by earlier than normal closure of some or all sutures of the infant skull. ... Congenital, Hereditary, and Neonatal Diseases and Abnormalities*Developmental abnormality*Congenital Systemic Disorder* ... Abnormality of the skull. MedGen UID: 488801. •Concept ID: C0235942. •. Anatomical Abnormality. ... Abnormality of the skull. MedGen UID: 488801. •Concept ID: C0235942. •. Anatomical Abnormality. ...
https://ncbi.nlm.nih.gov/medgen?term="Craniosynostosis syndrome"[Clinical Features] OR 1163[uid]

*  New Descriptors by Tree Subcategory - 2015

C16 (Congenital, Hereditary, and Neonatal Diseases and Abnormalities). Congenital Microtia. Hemimegalencephaly. Hernias, ... C10 (Nervous System Diseases). Allesthesia. Benign Paroxysmal Positional Vertigo. Cerebrospinal Fluid Leak. Hemimegalencephaly ... C13 (Female Urogenital Diseases and Pregnancy Complications). Atypical Hemolytic Uremic Syndrome. Atypical Squamous Cells of ... Hernias, Diaphragmatic, Congenital. Hyperlactatemia. Infant Death. Karoshi Death. Morphological and Microscopic Findings. ...
https://nlm.nih.gov/mesh/newbysub.html

*  Kitt Falk Petersen, MD > Internal Medicine | Yale School of...

Endocrine System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases ...
medicine.yale.edu/intmed/people/kitt_petersen-2.profile

*  BRENDA - Information on EC 2.4.1.267 - dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Analysis of multiple mutations in the hALG6 gene in a patient ... Congenital, Hereditary, and Neonatal Diseases and Abnormalities Employment of single-strand conformation polymorphism analysis ... Congenital, Hereditary, and Neonatal Diseases and Abnormalities Frequency Determination of ?-1,3 Glucosyltransferase p.Y131H ... frequent natural variant, the cause of congenital disorder of glycosylation-Ic (CDG-Ic). One patient with typical CDG-Ic ...
brenda-enzymes.org/enzyme.php?ecno=2.4.1.267

*  "Histone deacetylase 3 coordinates deacetylase-independent epigenetic s" by Sara L. Lewandowski, Harish P. Janardhan et al.

About two-thirds of human congenital heart disease (CHD) involves second heart field (SHF) derived structures. Histone- ... Cardiovascular Diseases , Cell Biology , Congenital, Hereditary, and Neonatal Diseases and Abnormalities , Developmental ... About two-thirds of human congenital heart disease (CHD) involves second heart field (SHF) derived structures. Histone- ... Molecular bases of disease, cardiac development, chromatin regulation, development, epigenetics, gene regulation ...
escholarship.umassmed.edu/gsbs_sp/1950/

*  "Infection control in cystic fibrosis: share and share alike" by Brian P. O'Sullivan and Christopher M. Sassetti

Congenital, Hereditary, and Neonatal Diseases and Abnormalities , Medical Microbiology , Microbiology , Respiratory Tract ...
escholarship.umassmed.edu/faculty_pubs/31/

*  Doctors <span class="caret"></span>

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Neoplasms; Pathological Conditions, ... Genital Diseases, Male; Kidney Diseases; Prostatic Neoplasms; Ureteral Diseases; Urethral Diseases; Urinary Bladder Diseases; ... Congenital Abnormalities; Developmental Biology; Molecular Biology; Pediatrics; Urologic Diseases; Urology Clinical Interests. ... Delivery of Health Care; Health Services Research; Kidney Diseases; Prostatic Neoplasms; Ureteral Diseases; Urinary Bladder ...
urology.med.yale.edu/doctors/index.aspx

*  JoVE | Peer Reviewed Scientific Video Journal - Methods and Protocols

Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial development, cranial neural crest, confocal ... Developmental Biology, Issue 79, Craniofacial Abnormalities, Jaw Abnormalities, Cleft Palate, Craniofacial Abnormalities, ... Transmission of the etiologic agent of Lyme disease, Borrelia burgdorferi, occurs by the attachment and blood feeding of Ixodes ... Two animal models, mice and nonhuman primates, are most commonly used for Lyme disease studies involving tick feeding. We ...
https://jove.com/visualize/abstract/21887229/hard-object-feeding-sooty-mangabeys-cercocebus-atys-interpretation

*  Results for: Subject:Prognosis | EthicShare Community

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1). *Cuspid (1). *Cyclophosphamide (1) ... 6. Neonatal intensive care: decision making in the face of prognostic uncertainty. ...
https://ethicshare.org/publications/(subject_parametric:"Prognosis")?filters=sm_cck_field_subtype:"Case Report" is_cck_field_year_published:1998&subject=Prognosis&sc=advanced

*  Results for: /NewsMagazine | EthicShare Community

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (39). *Terminally Ill (39). *Biomedical Research (37) ...
ethicshare.org/publications/%2FNewsMagazine?filters=sm_cck_field_subject:"Social Control, Formal"&solrsort=ds_cck_field_datetime_published desc

*  Fetal Growth Retardation - Intrauterine Growth Retardation Summary Report | CureHunter

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 668*Fetal Diseases: 626*Fetal Growth Retardation: 3246* ... Disease Context: Research Results. *Female Urogenital Diseases and Pregnancy Complications*Pregnancy Complications: 986*Fetal ...
curehunter.com/public/keywordSummaryD005317-Fetal-Growth-Retardation-Intrauterine-Growth-Retardation.do

*  Results for: /NewsMagazine | EthicShare Community

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (37). *Health Care Rationing (37) ...
ethicshare.org/publications/%2FNewsMagazine?filters=sm_cck_field_subject:"Federal Government"&solrsort=ds_cck_field_datetime_published desc

*  Olivopontocerebellar Atrophies - Olivopontocerebellar Atrophy Summary Report | CureHunter

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 668*Inborn Genetic Diseases: 842*Nervous System ... Disease Context: Research Results. *Nervous System Diseases: 6158*Neurodegenerative Diseases: 16953*Multiple System Atrophy: ... Brain Diseases: 2114*Cerebellar Diseases: 385*Spinocerebellar Degenerations: 244*Olivopontocerebellar Atrophies: 166* ... and hereditary cortical cerebellar atrophy (H-CCA)), and multiple system form (multiple system atrophy (MSA) and hereditary ...
curehunter.com/public/keywordSummaryD009849-Olivopontocerebellar-Atrophies-Olivopontocerebellar-Atrophy.do

*  Anakinra to Treat Patients With Neonatal Onset Multisystem Inflammatory Disease - Full Text View - ClinicalTrials.gov

Congenital Abnormalities. Urticaria. Joint Diseases. Cryopyrin-Associated Periodic Syndromes. Papilledema. Arthropathy, ... Immune System Diseases. Musculoskeletal Diseases. Hereditary Autoinflammatory Diseases. Genetic Diseases, Inborn. Skin Diseases ... Optic Nerve Diseases. Cranial Nerve Diseases. Nervous System Diseases. Eye Diseases. Interleukin 1 Receptor Antagonist Protein ... Abnormalities. Arthropathy. Urticaria. Papilledema. Auto-Inflammation. Inflammatory Disease. Neonatal Onset Multisystem ...
https://clinicaltrials.gov/ct2/show/NCT00069329?recr=Open&cond="Nervous System Malformations"&rank=1

*  Recent questions and answers in Tuberculosis, Lymph Node - lookformedical.com

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (8) * Skin and Connective Tissue Diseases (14) ... Diseases (562) * Bacterial Infections and Mycoses (27) * Bacterial Infections (16) * Bacteremia (1) ...
https://lookformedical.com/answers/en/diseases/bacterial-infections-and-mycoses/bacterial-infections/gram-positive-bacterial-infections/actinomycetales-infections/mycobacterium-infections/tuberculosis/tuberculosis-lymph-node

*  Make asthma SIMPLE for your patients | Feature | Pharmaceutical Journal

Animal diseases *. Cancer *. Cardiovascular diseases *. Congenital, hereditary, and neonatal diseases and abnormalities ... support groups for people with respiratory disease throughout the UK, with disease specific information available to download ... Type 2 diabetes in children and young people: extending our reach to prevent disease in those most at risk 19 SEP 2017 14:52 ... In around two-thirds of children with asthma, the disease remits in the early teenage years, only to relapse, in about a third ...
pharmaceutical-journal.com/news-and-analysis/features/make-asthma-simple-for-your-patients/11138140.article

*  Anemia - Hemolytic Pathway Map - PrimePCR | Life Science | Bio-Rad

Congenital, hereditary, and neonatal diseases and abnormalities , Anemia - Hemolytic ... Disease State Panels. PrimePCR disease state panels were designed by referencing the National Library of Medicine database. ... For diseases with a large number of gene targets, multiple tiered plates are available. Tier 1 plates represent the highest ... Disease state panels allow for the thorough investigation of differentially expressed genes within a specified pathology. ...
bio-rad.com/en-us/prime-pcr-assays/pathway/anemia-hemolytic

*  Hepatic Fibrosis, Congenital | CTD

Hepatic Fibrosis, Congenital 2.. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities ← Genetic Diseases ... Diseases ← Digestive System Diseases ← Liver Diseases ← Liver Cirrhosis ← ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ... Congenital Fibrose Liver , Congenital Hepatic Fibrosis Categories Digestive system disease , Genetic disease (inborn) ...
ctdbase.org/detail.go?type=disease&acc=MESH:C562378

*  Congenital Disorder Of Glycosylation, Type IIF | CTD

DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities ← Genetic Diseases, Inborn ← Metabolism, Inborn ... Congenital Disorder Of Glycosylation, Type IIF 2.. Diseases ← Nutritional and Metabolic Diseases ← Metabolic Diseases ← ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ...
ctdbase.org/detail.go?type=disease&acc=MESH:C567040

*  Acetylcarnitine deficiency | CTD

DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities ← Genetic Diseases, Inborn ← Metabolism, Inborn ... Diseases ← Nutritional and Metabolic Diseases ← Metabolic Diseases ← Metabolism, Inborn Errors ← Acetylcarnitine deficiency ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ...
ctdbase.org/detail.go?type=disease&acc=MESH:C536006

*  Glucose-6-phosphate translocase deficiency | CTD

DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities ← Genetic Diseases, Inborn ← Metabolism, Inborn ... Glycogen Storage Disease Type I ← Glucose-6-phosphate translocase deficiency 2.. Diseases ← Nutritional and Metabolic Diseases ... Metabolic Diseases ← Metabolism, Inborn Errors ← Carbohydrate Metabolism, Inborn Errors ← Glycogen Storage Disease ← Glycogen ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ...
ctdbase.org/detail.go?type=disease&acc=MESH:C536831

*  Cytochrome-c Oxidase Deficiency | CTD

DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities ← Genetic Diseases, Inborn ← Metabolism, Inborn ... Diseases ← Nutritional and Metabolic Diseases ← Metabolic Diseases ← Mitochondrial Diseases ← Cytochrome-c Oxidase Deficiency ... A disease that results from a congenital defect in ELECTRON TRANSPORT COMPLEX IV. Defects in ELECTRON TRANSPORT COMPLEX IV can ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ...
ctdbase.org/detail.go?type=disease&acc=MESH:D030401

*  Brugada Syndrome 3 | CTD

DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities ← Genetic Diseases, Inborn ← Brugada Syndrome ← ... Diseases ← Cardiovascular Diseases ← Heart Diseases ← Arrhythmias, Cardiac ← Brugada Syndrome ← Brugada Syndrome 3 ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ...
ctdbase.org/detail.go?type=disease&acc=MESH:C567509

*  MICROPHTHALMIA, ISOLATED 6 | CTD

DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesCongenital Abnormalities ← Eye Abnormalities ← ... Diseases ← Eye Diseases ← Eye Abnormalities ← Microphthalmos ← MICROPHTHALMIA, ISOLATED 6 2.. ... associated diseases · associated exposure references Home , Site Map , FAQ , Contact Us , Cite Us , Legal Notices , Downloads ...
ctdbase.org/detail.go?type=disease&acc=OMIM:613517

(1/7) Unfinished feticide: the ethical problems.

Dr. Jansen's paper raises three main issues. The one with which he himself is most concerned is the question of which methods of abortion are ethically right, and whether methods which risk the birth of a damaged baby are wrong. But there are two others: first, how the (originally unintended) birth of a live but damaged child alters the moral situation, and secondly, whether the overcoming of sterility by inducing a multiple pregnancy in which some of the fetuses have to be killed in order for any of them to survive is at all morally acceptable.  (+info)

(2/7) Unfinished feticide: a legal commentary.

Jansen expresses concern as to the legal implications of both selective reduction of pregnancy and unsuccessful attempts at termination of pregnancy using mifepristone. This commentary examines the legality of both procedures and concludes that Jansen is over-optimistic in his belief that neither procedure is likely to fall foul of the criminal laws on induced abortion. By contrast his anxieties about civil liability arising from the subsequent live birth of a damaged infant are, it is suggested, unnecessarily pessimistic. Such an action is most unlikely to succeed if brought by the infant herself and any claim on the part of the mother will normally be dependent on proof of negligence. The commentary focusses on the law in England with relevant references to other common law jurisdictions.  (+info)

(3/7) Paternalism versus autonomy: medical opinion and ethical questions in the treatment of defective neonates.

 (+info)

(4/7) Death by judiciary order.

 (+info)

(5/7) No right to sue for "wrongful life.

 (+info)

(6/7) Supplementary annual report of Council, 1982-1983: medical ethics.

 (+info)

(7/7) One man's burden.

 (+info)



disorders


  • fibroblasts from an ALG6-congenital disorders of glycosylation patient that carries the A333V mutation on the maternal ALG6 allele and the S308R and Y131H mutations on the paternal ALG6 allele assemble Dol-PP-GlcNAc2Man9 as the largest oligosaccharide donor. (brenda-enzymes.org)

genes


  • Disease state panels allow for the thorough investigation of differentially expressed genes within a specified pathology. (bio-rad.com)

Symptoms


  • Immune suppressing medicines commonly used to treat other pediatric rheumatologic diseases do not suppress NOMID symptoms and, if used long-term and in high doses, can cause harmful side effects. (clinicaltrials.gov)
  • The severity of the main symptoms of the disease were scored on a scale from 0 (no symptoms) to 4 (highest severity) on a daily basis using a diary. (clinicaltrials.gov)

chronic


  • A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. (labome.org)
  • This study will evaluate the safety and effectiveness of anakinra (Kineret) for treating patients with neonatal-onset multisystem inflammatory disease (NOMID), also known as chronic infantile neurological, cutaneous and arthropathy (CINCA) syndrome. (clinicaltrials.gov)

human


  • About two-thirds of human congenital heart disease (CHD) involves second heart field (SHF) derived structures. (umassmed.edu)