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17 Possible Causes for Anemia, Overfolded Superior Helix

  • Propionic Acidemia

    There was mild plagiocephaly and overfolding of the superior helix of each ear. The lower lip had loss of tissue in 2 lateral clefts with bulbous tissue in the center.[jamanetwork.com] Anemia was corrected, and the growth rate and mental development improved significantly.[ncbi.nlm.nih.gov] Commonly reported findings included seizures, arrhythmia, leucopenia, and anemia. Developmental and cognitive disabilities were reported in the majority of individuals.[ncbi.nlm.nih.gov]

  • Baller-Gerold Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[jmg.bmj.com] Clinical manifestations and chromosome breakage, consistent with Fanconi anemia, in patients with a prior diagnosis of either Baller-Gerold syndrome, reported earlier in one[ncbi.nlm.nih.gov] Other differential diagnoses include Roberts syndrome and Fanconi anemia, which are frequently associated with radial ray anomalies but rarely with craniosynostosis, and Saethre-Chotzen[orpha.net]

  • Pallister W Syndrome

    superior helix and small anthelix, sometimes cupped, with preauricular tags (fig 1 ).[jmg.bmj.com] […] result of these combined deficiencies, children with Wiskott-Aldrich syndrome are also at elevated risk for developing: autoimmune attack on the blood cells (autoimmune anemia[childrenshospital.org] Other complications that can be caused by nephrotic syndrome include: Anemia Heart disease High blood pressure Fluid buildup Acute kidney injury Kidney failure /ESRD Return[kidneyfund.org]

  • Branchio-Oculo-Facial Syndrome

    […] with hypoplastic superior helix, posterior and preauricular pit, supraauricular sinuses, conductive hearing loss secondary to fusion of the middle ear ossicles), the eyes[accessanesthesiology.mhmedical.com] Dry ice used to keep food cold, pyrethroid Pesticides Pre-existing illness—such as anemia, asthma, COPD, and coronary arterial disease—the stresses of flight could exacerbate[wikivisually.com] A CELLULE FALCIFORMI BLACKFAN-DIAMOND ANEMIA DI ANEMIA CONGENITA IPOPLASTICA FANCONI ANEMIA DI PANCITOPENIA DI FANCONI ANEMIE SIDEROBLASTICHE RD0010 SINDROME EMOLITICO UREMICA[studioassociatoanalisi.it]

  • Camptodactyly Syndrome Guadalajara Type 1

    The disorder is characterized by bruising, fatigue, anemia, low blood platelet count and enlargement of the liver and spleen, and is caused by a hereditary deficiency of the[checkrare.com]

  • Kleiner Holmes Syndrome

    superior helix; Deficient auricle; Hypertelorism; Megalophthalmos; Gingival hyperplasia; Prenatal teeth; Bell-shaped thorax; Hypoplastic clavicles; Decreased mineralization[panelapp.genomicsengland.co.uk] Stay current on the developments and research surrounding neonatal anemia from the entirely new chapter on Blood and Hematopoietic System highlights.[books.google.ro] Syndrome Tetrasomy X Thai Symphalangism Syndrome Thakker Donnai Syndrome THAUVIN-ROBINET-FAIVRE SYNDROME Theodor Hertz Goodman Syndrome thiamine-responsive megaloblastic anemia[rgd.mcw.edu]

  • FGFR2-Related Bent Bone Dysplasia

    […] syndrome1 Adams-Oliver Catel-Manzke syndrome Limb hypoplasia reduction defects group This includes the following conditions: Ulnar-mammary syndrome de Lange syndrome Fanconi anemia[emedicine.medscape.com] , complementation group C; FANCC Sequencing of all coding exons of the gene - - 1.7 FANCG Fanconi anemia Sequencing of all coding exons of the gene - - 1.9 FAS Autoimmune[cegat.de] […] neurologic cutaneous articular syndrome Sterile multifocal osteomyelitis, periostitis, and pustulosis Chronic recurrent multifocal osteomyelitis with congenital dyserythropoietic anemia[emedicine.medscape.com]

  • Coffin-Lowry Syndrome

    superior helix [ Graham et al 1998 ].[ncbi.nlm.nih.gov] A CELLULE FALCIFORMI BLACKFAN-DIAMOND, ANEMIA DI ANEMIA CONGENITA IPOPLASTICA FANCONI, ANEMIA DI PANCITOPENIA DI FANCONI ANEMIE SIDEROBLASTICHE METAEMOGLOBINEMIA DA DEFICIT[amaram.it] […] macrocephaly; constipation that may be associated with anal anomalies; broad thumbs and halluces; prominent fingertip pads; and small, rounded, cupped ears that often have an overfolded[ncbi.nlm.nih.gov]

  • Kaufman Oculocerebrofacial Syndrome

    Symptoms INHERITANCE: Autosomal dominant HEAD AND NECK: [Head]; Open metopic suture; [Face]; Midface hypoplasia; Micrognathia; [Ears]; Low-set ears; Overfolded superior helix[findzebra.com] Dry ice used to keep food cold, pyrethroid Pesticides Pre-existing illness—such as anemia, asthma, COPD, and coronary arterial disease—the stresses of flight could exacerbate[wikivisually.com] Congenital hypothyroidism Cornelia de Lange syndrome Diffuse cutaneous systemic sclerosis Duchenne muscular dystrophy Early-onset autosomal dominant Alzheimer disease Fanconi anemia[se-atlas.de]

  • Auriculocondylar Syndrome

    Narrow mouth Overfolding of the superior helices Postauricular skin tag Posteriorly rotated ears Preauricular skin tag Round face Stenosis of the external auditory canal[dovemed.com] , Dyserythropoietic, Congenital , see congenital dyserythropoietic anemia Anemia, hereditary sideroblastic , see X-linked sideroblastic anemia anemia, hypochromic microcytic[herenciageneticayenfermedad.blogspot.com] helix 0008559 Impaired mastication Chewing difficulties Chewing difficulty Difficulty chewing [ more ] 0005216 Low-set ears Low set ears Lowset ears [ more ] 0000369 Overfolding[rarediseases.info.nih.gov]

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