Hypertension, and Hodgkin lymphoma

Diseases related with Hypertension and Hodgkin lymphoma

In the following list you will find some of the most common rare diseases related to Hypertension and Hodgkin lymphoma that can help you solving undiagnosed cases.

Top matches:

Dyskeratosis congenita is an inherited bone marrow failure syndrome classically characterized by the triad of mucosal leukoplakia, nail dysplasia, and abnormal skin pigmentation. Affected individuals have an increased risk of aplastic anemia and malignancy. Less common features include epiphora, premature gray hair, microcephaly, developmental delay, and pulmonary fibrosis, among others. The phenotype is highly variable. All affected individuals have shortened telomeres due to a defect in telomere maintenance (summary by Savage et al., 2008).For a discussion of genetic heterogeneity of dyskeratosis congenita, see DCKA1 (OMIM ).

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3

Cartilage-hair hypoplasia is a disease affecting the bone metaphyses causing small stature from birth.

CARTILAGE-HAIR HYPOPLASIA Is also known as autosomal recessive metaphyseal chondrodysplasia|metaphyseal chondrodysplasia, mckusick type

Related symptoms:

  • Intellectual disability
  • Short stature
  • Scoliosis
  • Growth delay
  • Neoplasm


SOURCES: OMIM ORPHANET MENDELIAN

More info about CARTILAGE-HAIR HYPOPLASIA

The Heidelberg histologic classification of renal cell tumors subdivides renal cell tumors into benign and malignant parenchymal neoplasms and, where possible, limits each subcategory to the most common documented genetic abnormalities (Kovacs et al., 1997). Malignant tumors are subclassified into common or conventional renal cell carcinoma (clear cell); papillary renal cell carcinoma; chromophobe renal cell carcinoma; collecting duct carcinoma, with medullary carcinoma of the kidney; and unclassified renal cell carcinoma. The common or conventional type accounts for about 75% of renal cell neoplasms and is characterized genetically by a highly specific deletion of chromosome 3p. Papillary renal cell carcinoma (see {605074}) accounts for about 10% of renal cell tumors. Chromophobe renal cell carcinoma accounts for approximately 5% of renal cell neoplasms. Genetically, chromophobe RCC is characterized by a combination of loss of heterozygosity of chromosomes 1, 2, 6, 10, 13, 17, and 21 and hypodiploid DNA content. Collecting duct carcinoma accounts for about 1% of renal cell carcinoma.Renal cell carcinoma occurs nearly twice as often in men as in women; incidence in the United States is equivalent among whites and blacks. Cigarette smoking doubles the likelihood of renal cell carcinoma and contributes to as many as one-third of cases. Obesity is also a risk factor, particularly in women. Other risk factors include hypertension, unopposed estrogen therapy, and occupational exposure to petroleum products, heavy metals, or asbestos (summary by Motzer et al., 1996). Genetic Heterogeneity of Renal Cell CarcinomaGermline mutation resulting in nonpapillary renal cell carcinoma of the clear cell and chromophobe type occurs in the HNF1A gene (OMIM ) and the HNF1B gene (OMIM ).Somatic mutations in renal cell carcinomas occur in the VHL gene (OMIM ), the TRC8 gene (OMIM ), the OGG1 gene (OMIM ), the ARMET gene (OMIM ), the FLCN gene (OMIM ), and the BAP1 gene (OMIM ).See also RCCX1 (OMIM ) for a discussion of renal cell carcinoma associated with translocations of chromosome Xp11.2 involving the TFE3 gene (OMIM ).For a discussion of papillary renal cell carcinoma, see RCCP1 (OMIM ). Occurrence of Renal Cell Carcinoma in Other DisordersVon Hippel-Lindau syndrome (OMIM ) is a familial multicancer syndrome in which there is a susceptibility to a variety of neoplasms, including renal cell carcinoma of clear cell histology and renal cysts. A syndrome of predisposition to uterine leiomyomas and papillary renal cell carcinoma has been reported (OMIM ). Medullary carcinoma of the kidney is believed to arise from the collecting ducts of the renal medulla and is associated with sickle cell trait (OMIM ) (Kovacs et al., 1997). Renal cell carcinoma occurs in patients with the Birt-Hogg-Dube syndrome (OMIM ).Bertolotto et al. (2011) identified a missense mutation in the MITF (OMIM ) gene that increases the risk of renal cell carcinoma with or without malignant melanoma (CMM8 ).

RENAL CELL CARCINOMA, NONPAPILLARY; RCC Is also known as hypernephroma|adenocarcinoma of kidney

Related symptoms:

  • Neoplasm
  • Hypertension
  • Obesity
  • Carcinoma
  • Falls


SOURCES: OMIM ORPHANET MENDELIAN

More info about RENAL CELL CARCINOMA, NONPAPILLARY; RCC

Other less relevant matches:

Essential thrombocythemia (ET) is a myeloproliferative neoplasm (MPN, see this term) characterized by a sustained elevation of platelet number (> 450 x 109/L) with a tendency for thrombosis and hemorrhage.

ESSENTIAL THROMBOCYTHEMIA Is also known as thrombocytosis 1|essential thrombocytosis|et

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system
  • Respiratory distress


SOURCES: ORPHANET OMIM MENDELIAN

More info about ESSENTIAL THROMBOCYTHEMIA

Low match KAPOSI SARCOMA

Kaposi sarcoma (KS) is a rare human herpes virus 8 (HHV-8)-induced endothelial inflammatory neoplasm that develops is various clinically distinct settings, manifesting mostly as cutaneous lesions, or mucosal or visceral involvement.

KAPOSI SARCOMA Is also known as multiple idiopathic pigmented hemangiosarcoma, susceptibility to

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MENDELIAN

More info about KAPOSI SARCOMA

Severe combined immunodeficiency (SCID) due to adenosine deaminase (ADA) deficiency is a form of SCID characterized by profound lymphopenia and very low immunoglobulin levels of all isotypes resulting in severe and recurrent opportunistic infections.

SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY Is also known as ada deficiency|ada-scid|scid due to adenosine deaminase deficiency|scid due to ada deficiency|scid due to ada deficiency, early-onset

Related symptoms:

  • Global developmental delay
  • Failure to thrive
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY

Achondroplasia is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and midface hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, genu varum, and trident hand (summary by Bellus et al., 1995).

Related symptoms:

  • Intellectual disability
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Scoliosis


SOURCES: MESH OMIM MENDELIAN

More info about ACHONDROPLASIA; ACH

Schimke immuno-osseous dysplasia (SIOD) is a multisystem disorder characterized by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and glomerulonephritis with nephrotic syndrome.

SCHIMKE IMMUNO-OSSEOUS DYSPLASIA Is also known as immunoosseous dysplasia, schimke type|schimke syndrome|spondyloepiphyseal dysplasia-nephrotic syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Scoliosis
  • Growth delay


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about SCHIMKE IMMUNO-OSSEOUS DYSPLASIA

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia is a rare, genetic, polymalformative syndrome with increased risk of developing cancer characterized by a Noonan-like phenotype, including typical dysmorphic facial features (i.e. high forehead, hypertelorism, downslanting palpebral fissures, ptosis, low-set ears, prominent philtrum and short neck with or without pterygium colli), thoracic abnormalities, congenital heart defects and short stature, associated with a very frequent ocurrence of juvenile myelomonocytic leukemia. Developmental delay, ectodermal anomalies, joint laxity, and hypotonia may also be associated.

NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA Is also known as cbl mutation-associated syndrome|noonan syndrome-like disorder with jmml|cbl syndrome

Related symptoms:

  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly
  • Growth delay


SOURCES: ORPHANET OMIM MENDELIAN

More info about NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA

Neurofibromatosis type I is an autosomal dominant disorder characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin. Individuals with the disorder have increased susceptibility to the development of benign and malignant tumors. NF1 is sometimes referred to as 'peripheral neurofibromatosis.' The worldwide incidence of NF1 is 1 in 2,500 to 1 in 3,000 individuals (reviews by Shen et al., 1996 and Williams et al., 2009).Type II neurofibromatosis (NF2 ) is a genetically distinct disorder caused by mutation in the gene encoding merlin (NF2 ) on chromosome 22q12. NF2, sometimes known as 'central neurofibromatosis,' is characterized by bilateral acoustic neuroma and meningioma, but few skin lesions or neurofibromas (Rouleau et al., 1993).Some patients with homozygous or compound heterozygous mutations in mismatch repair genes (see, e.g., MLH1; {120436} and MSH2; {609309}) have a phenotype characterized by early onset malignancies and mild features of NF1, especially cafe-au-lait spots; this is known as the mismatch repair cancer syndrome (OMIM ), sometimes referred to as brain tumor-polyposis syndrome-1 or Turcot syndrome. These patients typically do not have germline mutations in the NF1 gene, although a study by Wang et al. (2003) suggested that biallelic mutations in mismatch repair genes may cause somatic mutations in the NF1 gene, perhaps resulting in isolated features resembling NF1.See also Legius syndrome (OMIM ), a genetically distinct disorder with a similar phenotype to NF1.

NEUROFIBROMATOSIS TYPE 1 DUE TO NF1 MUTATION OR INTRAGENIC DELETION Is also known as von recklinghausen disease due to nf1 mutation or intragenic deletion|neurofibromatosis, peripheral type|von recklinghausen disease

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Scoliosis
  • Hypertelorism


SOURCES: ORPHANET OMIM MENDELIAN

More info about NEUROFIBROMATOSIS TYPE 1 DUE TO NF1 MUTATION OR INTRAGENIC DELETION

Top 5 symptoms//phenotypes associated to Hypertension and Hodgkin lymphoma

Symptoms // Phenotype % cases
Lymphoma Very Common - Between 80% and 100% cases
Short stature Common - Between 50% and 80% cases
Neoplasm Uncommon - Between 30% and 50% cases
Growth delay Uncommon - Between 30% and 50% cases
Anemia Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Hypertension and Hodgkin lymphoma. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Abnormality of the skeletal system Leukemia Diarrhea Splenomegaly Pneumonia Abnormal lung morphology Fine hair Intellectual disability Scoliosis Gastrointestinal hemorrhage Cognitive impairment Cellular immunodeficiency Depressed nasal bridge Thrombocytopenia Delayed speech and language development B-cell lymphoma Immunodeficiency Cardiomyopathy Lumbar hyperlordosis Failure to thrive Abnormal facial shape Recurrent infections Hepatomegaly Motor delay Short neck Macrocephaly Tibial bowing Global developmental delay Hyperlordosis Abnormality of pelvic girdle bone morphology Abnormal form of the vertebral bodies Weight loss Neutropenia Lymphopenia Osteopenia Abnormality of skin pigmentation Malabsorption Headache Hepatosplenomegaly Pain

Rare Symptoms - Less than 30% cases

Rhizomelia Frontal bossing Atherosclerosis Aganglionic megacolon Overgrowth Overweight Abnormality of epiphysis morphology Genu varum Gastroesophageal reflux Reduced bone mineral density Thrombocytosis Scarring Generalized hypotonia Limited elbow extension Fever Disproportionate short-limb short stature Hydrocephalus Combined immunodeficiency Generalized joint laxity Abnormality of cardiovascular system morphology Edema Pulmonic stenosis Lymphedema Cafe-au-lait spot Sarcoma Hypermelanotic macule Gangrene Transient ischemic attack Myeloid leukemia Lymphoproliferative disorder Venous thrombosis Abnormality of the spleen Bruising susceptibility Paresthesia Multiple cafe-au-lait spots Respiratory distress Autoimmunity Platyspondyly Renal cell carcinoma Ptosis Hypertelorism Recurrent otitis media Falls Obesity Chronic myelogenous leukemia Abnormality of humoral immunity Abnormal T cell morphology Neonatal short-limb short stature Mucopolysacchariduria Abnormality of the metaphysis Neoplasm of the skin Anteverted nares Macrotia Sparse hair Low-set, posteriorly rotated ears Joint laxity Seizures Carcinoma Epicanthus Skeletal dysplasia Spondyloepiphyseal dysplasia Back pain Prominent forehead Severe short stature Hyperpigmentation of the skin Bone marrow hypocellularity Pulmonary fibrosis Dilatation Portal hypertension Myopia Respiratory insufficiency Pectus carinatum Epiphyseal dysplasia Aplastic anemia Joint hyperflexibility Astigmatism Hearing impairment Strabismus Microcephaly Micromelia Muscular hypotonia Cryptorchidism Joint hypermobility Intrauterine growth retardation Alopecia Visual impairment Osteoporosis Kyphosis Gait disturbance Cerebellar atrophy Downslanted palpebral fissures Optic atrophy Vomiting Anterior pituitary dysgenesis Premature arteriosclerosis Abnormality of the dentition Lumbar kyphosis in infancy Feeding difficulties Low-set ears Nephrosclerosis Lateral displacement of the femoral head Congestive heart failure Stage 5 chronic kidney disease Brain stem compression Atrial septal defect Polyhydramnios Thick vermilion border Abnormality of the foot Obstructive lung disease Hypermetropia Broad forehead Postnatal growth retardation Feeding difficulties in infancy Hypopnea High forehead Cervical cord compression Iritis Myopathy Posteriorly rotated ears Inguinal hernia Small foramen magnum Childhood onset short-limb short stature Abnormal immunoglobulin level Pectus excavatum Limited hip extension Trident hand Long philtrum Spinal stenosis with reduced interpedicular distance Myelitis Moyamoya phenomenon Subvalvular aortic stenosis Encephalomalacia Decreased testicular size Hypothyroidism Coarse hair Thin upper lip vermilion Azoospermia Hyperlipidemia Opacification of the corneal stroma Heterotopia Intellectual disability, profound Nephrotic syndrome Proteinuria Microdontia Abnormality of the kidney Encephalitis Waddling gait Premature birth Migraine Brain atrophy Developmental regression Stroke Gliosis Corneal opacity Hip dislocation Abnormal cerebellum morphology Nephropathy Chronic kidney disease Glomerulosclerosis Increased thyroid-stimulating hormone level Disproportionate short-trunk short stature Shallow acetabular fossae Steroid-resistant nephrotic syndrome Multiple lentigines Hypoplasia of the capital femoral epiphysis Arteriosclerosis Right ventricular cardiomyopathy Dentinogenesis imperfecta Bulbous nose Precocious atherosclerosis Cerebral ischemia Villous atrophy Ovoid vertebral bodies Dementia Thoracic kyphosis Abnormality of the vasculature Protuberant abdomen Glomerulopathy Renal insufficiency Steatorrhea High pitched voice Emphysema Focal segmental glomerulosclerosis Melanocytic nevus Nephritis Glomerulonephritis Highly arched eyebrow Prominent fingertip pads Ascites Freckling Anomalous pulmonary venous return Complete atrioventricular canal defect Pheochromocytoma Parathyroid adenoma Aqueductal stenosis Astrocytoma Brain neoplasm Myocardial fibrosis Neoplasm of the endocrine system Meningioma Increased reactive oxygen species production Severe vision loss Osteomalacia Neurofibromas Paraganglioma Hypophosphatemia Sensory axonal neuropathy Clitoral hypertrophy Precocious puberty Incoordination Breast carcinoma Spina bifida Sensorimotor neuropathy Bone pain Hypsarrhythmia Coarctation of aorta Mitral valve prolapse Abnormality of the cardiovascular system Tetralogy of Fallot Night sweats Carcinoid tumor Recurrent fractures Renovascular hypertension Tibial pseudoarthrosis Cerebral artery stenosis Arterial fibromuscular dysplasia Spinal neurofibromas Inguinal freckling Plexiform neurofibroma Acute promyelocytic leukemia Subcutaneous neurofibromas Optic nerve glioma Neurofibrosarcoma Neuroma Vestibular Schwannoma Embryonal rhabdomyosarcoma Axillary freckling Renal artery stenosis Rhabdomyosarcoma Single ventricle Pseudoarthrosis Soft tissue sarcoma Epigastric pain Dural ectasia Leiomyosarcoma Fibular bowing Gastrointestinal stroma tumor Neoplasm of the central nervous system Lisch nodules Renal phosphate wasting Schwannoma Glioma Nasolacrimal duct obstruction Specific learning disability Peripheral axonal neuropathy Triangular face Deep philtrum Hydrocele testis Facial hypotonia Abnormal eyebrow morphology Neurodevelopmental delay Decreased muscle mass Proximal placement of thumb Overfolded helix Cubitus valgus Abnormality of the thorax Pleural effusion Bilateral ptosis Failure to thrive in infancy Cholelithiasis Poor suck Bicuspid aortic valve Hypochromic microcytic anemia Torticollis Vasculitis Bilateral single transverse palmar creases Aortic valve stenosis Hydrops fetalis Mitral regurgitation Low posterior hairline Epistaxis Cyanosis Hip dysplasia Wide intermamillary distance Esotropia Webbed neck Abnormal bleeding Short attention span Chylothorax Facial asymmetry Intellectual disability, mild Genu valgum Pruritus Attention deficit hyperactivity disorder Paralysis Autistic behavior Hypertrophic cardiomyopathy Hypoglycemia Kyphoscoliosis Autism Glaucoma Hyperactivity Abnormal heart morphology Visual loss Depressivity Behavioral abnormality Broad toe Blindness Dysarthria Peripheral neuropathy Abnormality of the subarachnoid space Reduced factor X activity Reduced prothrombin activity Juvenile myelomonocytic leukemia Reduced factor XII activity Hypoplasia of olfactory tract Reduced factor IX activity Abnormality of the mediastinum Arteritis Pulmonary lymphangiectasia Monocytosis Cervical myelopathy Hyperreflexia Central sleep apnea Diaphyseal thickening Long fibula Narrow vertebral interpedicular distance Abnormality of the distal phalanx of finger Hypoplastic anemia Abnormally ossified vertebrae Abnormal bone ossification Congenital hypoplastic anemia Spinal dysraphism Large face Hypersplenism Normocytic anemia Abnormal diaphysis morphology Bronchiolitis Metaphyseal dysostosis Abnormality of chromosome stability Metaphyseal cupping Metaphyseal chondrodysplasia Aplasia/Hypoplasia affecting the eye Aplasia/Hypoplasia of the abdominal wall musculature Abnormality of the pancreas Tracheal stenosis Fair hair Heart block Upper limb undergrowth Exocrine pancreatic insufficiency Distal arthrogryposis Esophageal atresia Non-Hodgkin lymphoma Impaired lymphocyte transformation with phytohemagglutinin Anal stenosis Burkitt lymphoma Pulmonary embolism Prolonged bleeding time Leukocytosis Myelodysplasia Myocardial infarction Chest pain Vertigo Dyspnea Hemangioblastoma Cerebellar hemangioblastoma Small cell lung carcinoma Clear cell renal cell carcinoma Fibrosarcoma Sparse facial hair Papillary renal cell carcinoma Retinoblastoma Renal neoplasm Polycythemia Nephroblastoma Melanoma Renal cyst Pulmonary lymphoma Susceptibility to chickenpox Flaring of lower rib cage Absent pubertal growth spurt Biconvex vertebral bodies Severe T-cell immunodeficiency Hypoplasia of the odontoid process Macrocytic anemia Acute leukemia Oral leukoplakia Hypotrichosis Arthrogryposis multiplex congenita Abnormal cardiac septum morphology EEG abnormality Brachycephaly Constipation Delayed skeletal maturation Wide nasal bridge Pulmonary hemorrhage Reticulated skin pigmentation Phimosis Esophageal stricture Aseptic necrosis Short palm Interstitial pulmonary abnormality Premature graying of hair Epiphora Abnormal intestine morphology Leukopenia Pancytopenia Cerebral calcification Nail dysplasia Dry skin Nail dystrophy Retinopathy Cerebellar hypoplasia Ataxia Narrow chest Small hand Metaphyseal dysplasia Accelerated skeletal maturation High hypermetropia Abnormality of the hip bone Basal cell carcinoma Femoral bowing Mesomelia Short thorax Squamous cell carcinoma Cone-shaped epiphysis Metaphyseal widening Sacral dimple Reduced tendon reflexes Abnormal palate morphology Sparse eyelashes Hypopigmentation of the skin Hypocalcemia Short ribs Sparse and thin eyebrow Gingival overgrowth Abnormality of retinal pigmentation Bronchiectasis Bowing of the long bones Depressed nasal ridge Blue sclerae Abnormality of the ribs Convex nasal ridge Decreased antibody level in blood Postural instability Acrocyanosis Abnormality of the cerebral vasculature Thoracolumbar kyphosis Rigidity Recurrent urinary tract infections Osteoarthritis Tetraparesis Epidermal acanthosis Otitis media Sleep disturbance Oral cleft Confusion Apnea Cleft lip Abnormality of the nervous system Conductive hearing impairment Arthralgia Clonus Midface retrusion Malar flattening Ventriculomegaly Brachydactyly Flexion contracture Absent specific antibody response Reduced red cell adenosine deaminase activity Anti-thyroid peroxidase antibody positivity Lack of T cell function Severe B lymphocytopenia Absent tonsils Absence of lymph node germinal center Immunoglobulin IgG2 deficiency Short toe Paraparesis Cortical sclerosis Spinal cord compression Recurrent ear infections Myelopathy Hypoxemia Multiple epiphyseal dysplasia Cor pulmonale Abnormality of femur morphology Central apnea Dysuria Upper airway obstruction Communicating hydrocephalus Osteopetrosis Megalencephaly Obstructive sleep apnea Acanthosis nigricans Abnormality of the elbow Spinal canal stenosis Hip contracture Neuroblastoma Disproportionate short stature Bowel incontinence Short femoral neck Flared metaphysis Chronic otitis media Tinnitus Short long bone Infantile muscular hypotonia Sleep apnea Recurrent opportunistic infections Aplasia of the thymus Arterial thrombosis Skin rash Skin plaque Generalized lymphadenopathy Venous insufficiency Skin nodule Abnormality of the lower limb Abnormality of the gastrointestinal tract Macule Abnormal retinal morphology Hemangioma Pulmonary arterial hypertension Lymphadenopathy Papule Abnormality of the liver Neoplasm by anatomical site Encephalopathy Fatigue Increased megakaryocyte count Abnormal platelet aggregation Decreased mean platelet volume Abnormal platelet morphology Bloody diarrhea Myelofibrosis Abnormality of bone marrow cell morphology Amaurosis fugax Myeloproliferative disorder Impaired platelet aggregation Abnormal thrombocyte morphology Susceptibility to herpesvirus Recurrent respiratory infections Anterior rib cupping IgA deficiency Recurrent fungal infections Diffuse mesangial sclerosis B lymphocytopenia Decrease in T cell count Pulmonary insufficiency Increased IgE level IgM deficiency Allergy Verrucae Recurrent viral infections Recurrent lower respiratory tract infections Severe combined immunodeficiency Autoimmune thrombocytopenia Autoimmune hemolytic anemia Respiratory tract infection Malnutrition Recurrent upper respiratory tract infections Eosinophilia Leukoencephalopathy Purpura Recurrent bacterial infections Recurrent pneumonia Sinusitis Chronic diarrhea Inflammatory abnormality of the skin Hepatitis Asthma Sepsis Brow ptosis


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