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12 Possible Causes for Congenital Facial Anomaly, Luteinizing Hormone Low, Volvulus

  • CHARGE Syndrome

    Kabuki syndrome is a rare genetic disorder characterized by intellectual disability and multiple congenital anomalies, including short stature, peculiar facial appearance,[ncbi.nlm.nih.gov] Cecal volvulus occurring in a child with CHARGE syndrome is presented.[ncbi.nlm.nih.gov] […] amounts of luteinizing hormone (LH), follicle-stimulating hormone (FSH), or both. 24 Under normal circumstances, these hormones are released by the pituitary gland after[nursingcenter.com]

  • Acquired Porencephaly

    Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.[ncbi.nlm.nih.gov] […] hydroxyglutarate dehydrogenase 14q21.3 L-2-Hydroxyglutaric Aciduria, 2-Hydroxyglutaric Aciduria D-2-Hydroxyglutaric Aciduria L3MBTL3 l(3)mbt-like 3 (Drosophila) 6q23.1 Intestinal Volvulus[genecards.weizmann.ac.il] Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS.[ncbi.nlm.nih.gov]

  • Salti-Salem Syndrome

    Dysmorphism Muller Barth Menger Syndrome multiple congenital anomalies-hypotonia-seizures syndrome Myopathy, Cataract, Hypogonadism Syndrome NEURODEVELOPMENTAL DISORDER WITH[rgd.mcw.edu] * Duker Weiss Siber syndrome * Duodenal atresia * Duodenal atresia tetralogy of Fallot * Duodenal ulcer due to antral G-cell hyperfunction * Duodenojejunal atresia with volvulus[medicalgeek.com] Chemically, hCG is similar to luteinizing hormone (LH) as it stimulates testosterone production.[omicsonline.org]

  • OSLAM Syndrome

    VCFS, was originally described as the combination of palatal anomalies, often velopharyngeal incompetence (VPI), congenital heart disease (usually a ventricular septal defect[ncbi.nlm.nih.gov] Gangrenous or ischemic bowel segments may have to be removed if there is associated colonic volvulus.[radiopaedia.org] Laboratory studies show inappropriately low or normal serum concentration of LH (luteinizing hormone) and FSH (follicle stimulating hormone) in the presence of low circulating[omicsonline.org]

  • Congenital Clubbing

    […] tremorはばたき振戦 flatus放屁 food poisoning食中毒 free air 遊離ガス fulminant hepatitis劇症肝炎 fundus (fornix)胃底部(穹窿部) g gallbladder (Vesica fellea, Vesica biliaris) 胆嚢 gallbladder torsion (volvulus[tokyo-med.ac.jp] 97 thanks, 74 comments 16 Apr 2016 Thank Share Post Verified response multiple congenital anomalies. ...hydrocephalus, spina bifida, bilateral club foot, low set ears,?[dailyrounds.org] Other hormones like luteinizing hormone (LH), follicle stimulating hormone (FSH) as well as estrogen and progestogen gave low values depicting a hypogonadotropic hypogonadism[e-ijd.org]

  • Pallister W Syndrome

    , SNOMED-CT } Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder) {773643006, SNOMED-CT } Multiple malformation syndrome with facial-limb defects[phinvads.cdc.gov] McPherson Clemens syndrome 0 *Abnormalities, Multiple *Cleft Lip *Cleft Palate *Heart Defects, Congenital *Facies *Intestinal Volvulus.[reference.md] In addition, follicle-stimulating hormone and luteinizing hormone levels were low.[ajnr.org]

  • Nelson Syndrome

    Examples of these anatomical defects are seen in patients with Eustachian tube dysfunction and congenital anomalies such as Down syndrome, cleft palate, Townes and oral-facial-digital[aacijournal.biomedcentral.com] Rarely, sigmoid volvulus occurs 86.[nature.com] The endocrine tests suggested absent testicular function (low AMH, low to undetectable testosterone, high FSH and luteinizing hormone) so acquired bilateral anorchia was considered[scielo.br]

  • Perrault Syndrome 3

    […] cases of D-la described in this review had a history of SBS due to various causes including ischemic bowel, intestinal obstruction, congenital abnormalities, and midgut volvulus[hindawi.com] Congenital disorder of glycosylation, type Im 610768 D PAGT1 11q23.3 Congenital disorder of glycosylation, type Ij 608093 Myasthenic syndrome, congenital, 13, with tubular[institutobernabeu.com] A simple means of distinguishing between the 2 conditions is to measure serum follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels (elevated in POF and low[www1.cgmh.org.tw]

  • Ichthyosis-Intellectual Disability-Dwarfism-Renal Impairment Syndrome

    Hemifacial microsomia (HFM) is the second most common congenital facial anomaly after cleft lip/palate. The condition may vary from mild to severe.[radiopaedia.org] Abdominal pain and other complications including intussusception, volvulus and infarction have been described.[entokey.com] […] oculocerebrorenal syndrome Endocrine Luteinizing hormone resistance Endocrine Multiple endocrine neoplasia type 1 (MEN1) Endocrine Multiple endocrine neoplasia type 2 (MEN2[genomediagnosticsnijmegen.nl]

  • Skeletal Dysplasia - Intellectual Disability Syndrome

    Respiratory causes, including aspiration and pneumonia, are the most common primary causes (31%) followed by gastrointestinal disease, including obstruction/volvulus (19%)[patient.info] anomalies (MCA) Hartsfield syndrome Multiple congenital anomalies (MCA) Hereditary congenital facial paresis Multiple congenital anomalies (MCA) Hidrotic Ectodermal Dysplasia[genomediagnosticsnijmegen.nl] anomalies, finger camptodactyly, and joint hyperlaxity.[genome.jp]

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