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53 Possible Causes for Congenital Alopecia, Facial Hemiatrophy, Iron Deficiency Anemia

  • Tollner-Horst-Manzke Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] alopecia Autosomal dominant partial epilepsy with auditory features Autosomal dominant polycystic kidney disease - Not a rare disease Autosomal dominant pseudohypoaldosteronism[rarediseases.info.nih.gov] hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Fallot Complex with Severe[rgd.mcw.edu]

  • Rasmussen Syndrome

    Parry-Romberg syndrome (progressive facial hemiatrophy) is a unilateral, slowly progressive atrophy affecting the skin, subcutaneous tissues, muscles, and bones.[ncbi.nlm.nih.gov] A 9-year-old boy diagnosed as having Rasmussen syndrome had congenital IgA deficiency and juvenile alopecia.[ncbi.nlm.nih.gov] All routine laboratory investigations were normal except for the iron deficiency anemia (Hb 9.7g/dL, MCH 21 pg/cell, MCV 69 fL, RDW 14.9%) in the full blood count.[kenkyugroup.org]

  • Patterson Pseudoleprechaunism Syndrome

    Dysmorphism with Multiple Malformations facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome Faciogenital Dysplasia with[rgd.mcw.edu] alopecia, Stevanovic type - See Autosomal dominant palmoplantar keratoderma and congenital alopecia Palmoplantar keratoderma and sensorineural deafness - See Keratoderma[herenciageneticayenfermedad.blogspot.com] deficiency anemia after iron infusion: an analogy with Plummer Vinson syndrome. ( 27917348 ) Arya V...Ohri A 2016 17 Single-center prospective study of Plummer-Vinson syndrome[malacards.org]

  • Skin Atrophy

    hemiatrophy.[blackwellreference.com] Scarring alopecia, congenital absence of three toenails, and a scarlike lesion of the tongue were also present.[ncbi.nlm.nih.gov] The examples include diabetes mellitus, leukemia and lymphoma, kidney failure, liver diseases (obstructive jaundice), iron deficiency anemia, or hyperthyroidism.[fascrs.org]

  • Chudley-Rozdilsky Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome facial[rgd.mcw.edu] […] absence of the sternocleidomastoid muscle Congenital adrenal hyperplasia Congenital alopecia X-linked Congenital amegakaryocytic thrombocytopenia Congenital amputation Congenital[personalizedcause.com] Anemia from low levels of iron in the blood (iron deficiency anemia). What other names is Iron known by? Are there safety concerns? Dosing considerations for Iron.[nhha.org]

  • Congenital Hemihypertrophy

    […] hemihypertrophy and facial hemiatrophy are rare developmental anomalies.[jiaomr.in] […] epidermolytic hyperkeratosis,607602 CLDN1 Ichthyosis,leukocyte vacuoles,alopecia and sclerosing cholangitis,607626 CERS3 Ichtyosis, congenital, autosomal recessive 9, 615023[gsdseq.ir] […] structural asymmetry / facial hemiatrophy / facial hemihypertrophy - Macrostomia / big mouth - Polydactyly of toes - Syndactyly of toes - Telangiectasiae of the skin - Upper[csbg.cnb.csic.es]

  • Hereditary Hyperekplexia

    hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder Failed Back Surgery Syndrome Familial Antiphospholipid[rgd.mcw.edu] […] variant) FOXI1 (Enlarged vestibular aqueduct) FOXL2 (Blepharophimosis, epicanthus inversus, and ptosis, type 1) FOXN1 (T-cell immunodeficiency, congenital alopecia, and nail[en.praenatal-medizin.de] Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Alopecia, neurologic defects, and endocrinopathy syndrome Deficiency of butyryl-CoA dehydrogenase[amp.pharm.mssm.edu]

  • Craniorhiny

    FACIAL HEMIATROPHY  Atrophy of the soft tissues of half of the face i.e skin, muscles, bones, soft palate. 37 38.[slideshare.net] ; CCCA OMIM:217600 Central Cloudy Dystrophy of Francois; CCDF OMIM:117000 Central Core Disease of Muscle; CCD OMIM:209880 Central Hypoventilation Syndrome, Congenital; CCHS[informatics.jax.org] anemia, thalassemia, iron deficiency) • Antley-Bixler syndrome • Apert syndrome • Armendares syndrome • Asphyxiating thoracic dysplasia • Baller-Gerold syndrome • Beare-Stevenson[rrnursingschool.biz]

  • CAMFAK Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder[rgd.mcw.edu] […] megalocornea Stickler syndrome, type 2 Pitt-Hopkins syndrome Alopecia macular degeneration growth retardation Glycogen storage disease type 5 Hyperlipoproteinemia type 5[checkrare.com] Restless legs syndrome in Indian patients having iron deficiency anemia in a tertiary care hospital. Sleep Medicine. 2007, 8 (3): 247–51.[zh.wikipedia.org]

  • Dursun Syndrome

    Abnormalities, Kyphoscoliosis, and Mental Retardation facial hemiatrophy Facio Thoraco Genital Syndrome Faciocardiomelic Syndrome Faciocardiorenal Syndrome factitious disorder[rgd.mcw.edu] […] variant 613454 FOXN1 17q11.2 T-cell immunodeficiency, congenital alopecia, and nail dystrophy 601705 FOXP3 Xp11.23 Immunodysregulation, polyendocrinopathy, and enteropathy[institutobernabeu.com] […] syndrome, atypical, Thrombophilia due to thrombomodulin defect TMPRSS6 Iron-refractory iron deficiency anemia TPI1 Triosephosphate isomerase deficiency XRCC2 Hereditary breast[genda.com.ar]

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