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99 Possible Causes for Anemia, Mild Coxa Vara

  • Microcephalic Osteodysplastic Primordial Dwarfism Type II

    coxa vara.[] Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II Abstract We report a 4 month old male, 4th in order[] coxa vara, a sharp, high-pitched voice and a social personality (see Figure 1 ).[]

  • Osteomyelitis

    Similar to type IV Type VII Autosomal recessive Associated with rhizomelia and coxa vara Presentation Symptoms mild cases multiple fractures during childhood severe cases[] [Crossref] Mayo Clinic (2016) Diseases and Conditions- Sickle cell anemia.[] (due to anemia of chronic disease, sickle cell anemia etc which may give rise to non-healing ulcers.)[]

  • Shwachman Syndrome

    Skeletal manifestations include delayed bone age with marked carpal delay, broad cup-like anterior ribs, metaphyseal irregularities, and coxa vara with short femoral necks[] These patients, however, exhibited many features similar to other constitutional hematologic disease, such as Fanconi's anemia, which are atypical for Shwachman syndrome.[] […] syndrome, Blackfan-Diamond anemia, celiac disease, and autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (see these terms).[]

  • Coxa Vara

    A slight modification of this system includes: idiopathic: congenital: mild or severe coxa vara, with associated congenital anomalies: see associations developmental: progressive[] Sepper Roxadustat Treatment for Anemia in Patients Undergoing Long-Term Dialysis N. Chen et al. Roxadustat and Anemia of Chronic Kidney Disease J.[] Clinical features include mandibular prognathism, genu val-gum, anemia, hepatosplenomegaly, tendency to frac-ture,mandibular osteomyelitis,and dental anomalies (Burns et al[]

  • Radial Hemimelia

    […] arthrogryposis and causes loss of MCP extension Treatment : Stretching splints, soft tissue release /- EIP transfer Coxa Vara Type I Present at birth Rare Associated with[] —The "Picture of the Month" in the May issue of the Journal (page 583) shows a newborn infant under the diagnosis of Fanconi's anemia (chronic pancytopenia with multiple congenital[] […] spontaneously in the first year Treatment : Release at about 2 years Congenital contracture of 1st web Clasp thumb X-linked recessive Usually isolated Occasionally seen in mild[]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    vara ), and a foot deformity known as clubfoot.[] 1 Diamond-Blackfan anemia 10 Diamond-Blackfan anemia 3 Diamond-Blackfan anemia 5 Diamond-Blackfan anemia 7 Diamond-Blackfan anemia 8 Diamond-Blackfan anemia 9 Diffuse mesangial[] In the first group the changes are severe with absent ossification of the femoral neck and coxa vara.[]

  • Seckel Syndrome

    The radiological abnormalities in MOPDII are short limbs with preferential distal involvement, coxa vara, epiphysiolysis and metaphyseal flaring with V-shaped distal femora[] There have been several reports of associated hematological abnormalities and chromosomal breakage, findings suggestive of Fanconi anemia (FA).[] The 12-yr-old female had pancytopenia, which is seen occasionally in patients with Seckel syndrome and is also a feature of Fanconi anemia, a well-recognized autosomal recessive[]

  • Congenital Cortical Hyperostoses

    Coxa vara, long-bone bowing, hip and knee degenerative arthritis, and mandibular and long-bone osteomyelitis may also occur.[] The patient had hereditary hemolytic anemia with unstable hemoglobin of the Christchurch type.[] […] syndrome epicondylitis Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness Epiphyseal Dysplasia, Baumann Type Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia[]

  • Cystitis

    Coxa vara and mild spinal changes are also associated.[] […] are sensitive to nitrofurans; and in those with glucose-6-phosphate dehydrogenase (G6PD) deficiency. 2,17 While nitrofurantoin is safe in pregnancy, it can cause hemolytic anemia[] General debility Renal calculi or obstruction Recent hospitalization Urinary tract instrumentation or antibiotic therapy Diabetes mellitus Chronic nephropathy Sickle cell anemia[]

  • Spondyloepiphyseal Dysplasia Congenita

    Herein, we describe a unique case of SEDC with mild coxa vara (SEDC-M) caused by double de novo COL2A1 mutations located on the same allele.[] A CELLULE FALCIFORMI BLACKFAN-DIAMOND, ANEMIA DI ANEMIA CONGENITA IPOPLASTICA FANCONI, ANEMIA DI PANCITOPENIA DI FANCONI ANEMIE SIDEROBLASTICHE METAEMOGLOBINEMIA DA DEFICIT[] The 2 types of the disease are the mild coxa vara form, with height maintained (as in our patient) and the severe coxa vara form, with clinical short stature.[]

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