Intellectual disability, severe, and Ulcerative colitis

Diseases related with Intellectual disability, severe and Ulcerative colitis

In the following list you will find some of the most common rare diseases related to Intellectual disability, severe and Ulcerative colitis that can help you solving undiagnosed cases.

Top matches:

X-linked reticulate pigmentary disorder shows more severe manifestations in hemizygous males compared to heterozygous females. Affected males have early onset of recurrent respiratory infections and failure to thrive resulting from inflammatory gastroenteritis or colitis. Patients also show reticular pigmentation abnormalities of the skin and may develop corneal scarring. Carrier females may be unaffected or have only pigmentary abnormalities along the lines of Blaschko (summary by Starokadomskyy et al., 2016).

PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED; PDR Is also known as xlpdr

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Failure to thrive
  • Visual impairment


SOURCES: OMIM MENDELIAN

More info about PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED; PDR

Frontometaphyseal dysplasia (FMD) is a progressive sclerosing skeletal dysplasia characterized by supraorbital hyperostosis, undermodeling of the small bones, and small and large joint contractures, as well as extraskeletal developmental abnormalities, primarily of the cardiorespiratory system and genitourinary tract. Patients with FMD2 appear to have a propensity for keloid formation (summary by Wade et al., 2016).For a discussion of genetic heterogeneity of frontometaphyseal dysplasia, see FMD1 (OMIM ).

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Scoliosis
  • Hypertelorism
  • Sensorineural hearing impairment


SOURCES: OMIM MENDELIAN

More info about FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2

VELOCARDIOFACIAL SYNDROME Is also known as chromosome 22q11.2 deletion syndrome|shprintzen vcf syndrome|vcf syndrome|vcfs

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about VELOCARDIOFACIAL SYNDROME

Other less relevant matches:

BASAL CELL NEVUS SYNDROME; BCNS Is also known as nevoid basal cell carcinoma syndrome|gorlin-goltz syndrome|gorlin syndrome|nbccs|multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Microcephaly
  • Scoliosis
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about BASAL CELL NEVUS SYNDROME; BCNS

Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Goltz syndrome or focal dermal hypoplasia is characterized by a polymorphic cutaneous disorder and highly variable anomalies affecting the eyes, teeth, skeleton and the central nervous, urinary, gastrointestinal and cardiovascular systems.

FOCAL DERMAL HYPOPLASIA Is also known as dhof|goltz syndrome|goltz-gorlin syndrome|fodh

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about FOCAL DERMAL HYPOPLASIA

Pitt-Hopkins syndrome (PHS) is characterized by the association of intellectual deficit, characteristic facial dysmorphism and problems of abnormal and irregular breathing.

PITT-HOPKINS SYNDROME Is also known as encephalopathy, severe epileptic, with autonomic dysfunction|mental retardation, syndromal, with intermittent hyperventilation

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about PITT-HOPKINS SYNDROME

Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD, see this term), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect.

OCCIPITAL HORN SYNDROME Is also known as eds ix, formerly|eds ix|ehlers-danlos syndrome type ix|ehlers-danlos syndrome type 9|x-linked cutis laxa|ehlers-danlos syndrome, occipital horn type, formerly|eds9, formerly|cutis laxa, x-linked, formerly

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about OCCIPITAL HORN SYNDROME

The Cornelia de Lange syndrome (CDLS) is a multisystem malformation syndrome recognized primarily on the basis of characteristic facial dysmorphism, including low anterior hairline, arched eyebrows, synophrys, anteverted nares, maxillary prognathism, long philtrum, thin lips, and 'carp' mouth, in association with prenatal and postnatal growth retardation, mental retardation and, in many cases, upper limb anomalies. However, there is wide clinical variability in this disorder, with milder phenotypes that may be difficult to ascertain on the basis of physical features (summary by Rohatgi et al., 2010).Boyle et al. (2015) provided a detailed review of CDLS, including clinical features, diagnosis, and genetic counseling. Genetic Heterogeneity of Cornelia de Lange SyndromeAbout 50 to 60% of the cases of CDLS are due to mutation in the NIPBL gene (Musio et al., 2006; Rohatgi et al., 2010).One X-linked form of CDLS (CDLS2 ) is caused by mutation in the SMC1A gene (OMIM ), which accounts for about 5% of cases. Two milder variants of Cornelia de Lange syndrome have been identified: CDLS3 (OMIM ), caused by mutation in the SMC3 gene (OMIM ), and CDLS4 (OMIM ), caused by mutation in the RAD21 gene (OMIM ). All 4 genes, NIPBL, SMC1A, SMC3, and RAD21, encode components of the cohesin complex. Another X-linked form, CDLS5 (OMIM ), is caused by mutation in the HDAC8 gene (OMIM ), the vertebrate histone deacetylase of SMC3.

CORNELIA DE LANGE SYNDROME 1; CDLS1 Is also known as typus degenerativus amstelodamensis|brachmann-de lange syndrome|cdl|de lange syndrome|cdls|bdls

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about CORNELIA DE LANGE SYNDROME 1; CDLS1

Immunodeficiency due to ficolin3 deficiency is a rare, genetic, immunodeficiency due to a complement cascade protein anomaly characterized by low or undetectable serum ficolin3 levels, susceptibility to infections, and possibly autoimmunity. The presentation is variable, from perinatal necrotizing enterocolitis and recurrent skin infections with Staphylococcus aureus to childhood-onset recurrent pulmonary infections leading to brain abscesses and pulmonary fibrosis, to membranous nephropathy. In some patients, clinical consequences of ficolin3 deficiency were not clear.

IMMUNODEFICIENCY DUE TO FICOLIN3 DEFICIENCY Is also known as fcn3 deficiency|lectin complement activation pathway, defect in, 3|lcapd3

Related symptoms:

  • Intellectual disability
  • Microcephaly
  • Growth delay
  • Ventricular septal defect
  • Immunodeficiency


SOURCES: OMIM ORPHANET MENDELIAN

More info about IMMUNODEFICIENCY DUE TO FICOLIN3 DEFICIENCY

Top 5 symptoms//phenotypes associated to Intellectual disability, severe and Ulcerative colitis

Symptoms // Phenotype % cases
Intellectual disability Very Common - Between 80% and 100% cases
Scoliosis Common - Between 50% and 80% cases
Abnormality of the pinna Common - Between 50% and 80% cases
Microcephaly Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Intellectual disability, severe and Ulcerative colitis. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Hearing impairment

Uncommon Symptoms - Between 30% and 50% cases

Global developmental delay

Common Symptoms - More than 50% cases

Cryptorchidism

Uncommon Symptoms - Between 30% and 50% cases

High palate Generalized hypotonia Abnormality of the skeletal system Cleft palate Abnormal facial shape Strabismus Inguinal hernia Hernia Talipes equinovarus Growth delay Gastroesophageal reflux Depressed nasal bridge Short metatarsal Wide nasal bridge Hypertelorism Clinodactyly Specific learning disability Inflammation of the large intestine Failure to thrive Syndactyly Hiatus hernia Hydrocephalus Neoplasm Micrognathia Pneumonia Ventricular septal defect Abnormality of the dentition Scarring Short stature Muscular hypotonia Dislocated radial head Pulmonic stenosis Obesity Tapered finger Thick eyebrow Small hand Full cheeks Blue sclerae Cleft upper lip Short neck Bicuspid aortic valve Myopia Cognitive impairment Behavioral abnormality Aggressive behavior Intrauterine growth retardation Fever Abnormal heart morphology Autism Feeding difficulties Nystagmus Hyperactivity Umbilical hernia Retrognathia Delayed speech and language development Conductive hearing impairment Sleep disturbance Downslanted palpebral fissures Motor delay Respiratory tract infection Brachydactyly Ptosis Colitis Spina bifida Mandibular prognathia Camptodactyly Low-set ears Increased body weight Esophagitis Patent ductus arteriosus Pectus excavatum Intellectual disability, mild

Rare Symptoms - Less than 30% cases

Coloboma Abdominal pain Brachycephaly Microphthalmia Macrocephaly Papule Epicanthus Clubbing Supernumerary ribs Pain Ataxia Limited elbow extension Psychotic episodes Perimembranous ventricular septal defect Gastroparesis Abnormality of the sense of smell Echolalia Hypotrichosis Recurrent urinary tract infections Carious teeth Relative macrocephaly High, narrow palate Bradycardia Short ribs Iris coloboma Hypogonadotrophic hypogonadism Sparse hair Spina bifida occulta Cleft lip Telecanthus Cerebral calcification Proteinuria Hip dislocation Coarse facial features Vertebral fusion Arachnodactyly Long philtrum Proptosis Down-sloping shoulders Glaucoma Upslanted palpebral fissure Self-injurious behavior Dysphagia Narrow forehead Anteverted nares Spontaneous abortion Sleep apnea Poor suck Narrow nasal bridge Acrocyanosis Hypothermia Hand oligodactyly Clitoral hypoplasia Verrucae Optic atrophy Hyperhidrosis Pes planus Hydronephrosis Joint laxity Short clavicles Oligodactyly Ectrodactyly Toe syndactyly Hypoplastic nipples Delayed eruption of teeth Abnormality of digit Congenital diaphragmatic hernia Supernumerary nipple Renal hypoplasia Hip dysplasia Postnatal growth retardation Incoordination Narrow mouth Coarse hair Widely spaced teeth Hypertension Vomiting Kyphosis Dilatation Convex nasal ridge Prominent forehead Osteoporosis Truncus arteriosus Micropenis Weight loss Osteopenia Sepsis Thin upper lip vermilion Hypoglycemia Single transverse palmar crease Apnea Astigmatism Dolichocephaly Pruritus Prominent nasal bridge Genu valgum Autistic behavior Short palm Downturned corners of mouth Hypopigmentation of the skin Myelomeningocele Polydactyly Recurrent skin infections Anxiety Absent speech Short philtrum Thrombocytopenia Flexion contracture Hypospadias Sensorineural hearing impairment Enterocolitis Vesicoureteral reflux Hirsutism Amenorrhea Psychosis Low posterior hairline Failure to thrive in infancy Primary amenorrhea Open mouth Multicystic kidney dysplasia Narrow palpebral fissure Delayed puberty Broad nasal tip Nasal speech Anemia Pierre-Robin sequence Stridor Pyloric stenosis Deep philtrum Coxa valga Finger clinodactyly Congenital hip dislocation Cataract Hypoplasia of the corpus callosum Bifid uvula Pointed chin Atrial septal defect Low anterior hairline Webbed neck Immunodeficiency Recurrent infections Abnormality of cardiovascular system morphology Short metacarpal Arnold-Chiari malformation Decreased muscle mass Hyperpigmentation of the skin Visual loss Recurrent respiratory infections Dysarthria Diarrhea Photophobia Abnormality of skin pigmentation Chronic diarrhea Blindness Pes cavus Panhypopituitarism Hypoplastic male external genitalia Telangiectasia of the skin Protruding ear Anteriorly placed anus Midclavicular aplasia Fatigue Nephrotic syndrome Curly eyelashes Encephalopathy Absent hand Phocomelia Aplasia cutis congenita Peters anomaly Nephropathy Aplasia/Hypoplasia of the skin Facial cleft Deeply set eye Constipation Short sternum Gait ataxia Intellectual disability, moderate Hypermelanotic macule Macule Thick vermilion border Prominent nose Reduced number of teeth Abdominal distention Dermal atrophy Abnormality of the gastrointestinal tract Brittle hair Optic nerve coloboma Hand polydactyly Thick upper lip vermilion Recurrent hypoglycemia Ectopia lentis Ectropion Mixed hearing impairment Chorioretinal coloboma Abnormality of dental morphology Anophthalmia Mild short stature Severe global developmental delay Neurological speech impairment Open bite Membranous nephropathy Volvulus Recurrent lower respiratory tract infections Wide mouth Short finger Esophageal stenosis Hypertropia Midclavicular hypoplasia Hypoplastic radial head Foot polydactyly Total anomalous pulmonary venous return Duplication of internal organs Abnormality of hair texture Hypoplasia of the iris Split foot Abnormal cornea morphology Ureteral duplication Bifid nose Malrotation of colon Skin nodule Anomalous pulmonary venous return Aplasia/Hypoplasia of the lungs Inspiratory stridor Hypoplasia of teeth Cholangitis Stenosis of the external auditory canal Labial hypoplasia Abnormality of the larynx Otitis media with effusion Abnormality of the umbilicus Lower limb asymmetry Hypoplastic pelvis Duodenal atresia Acute hepatic failure Diastasis recti Papilloma Aniridia Giant cell tumor of bone Abnormality of the mediastinum Reduced renal corticomedullary differentiation Apocrine hidrocystoma Cholesteatoma Linear hyperpigmentation Ectopia cordis Bifid ureter Abnormal adipose tissue morphology Abnormality of the pulmonary vasculature Nonproductive cough Dysplastic tricuspid valve Osteopathia striata Cleft ala nasi Abnormal palmar dermatoglyphics Projectile vomiting Left-to-right shunt Caudal appendage Ridged fingernail Absence of the sacrum Patchy alopecia Upper limb asymmetry Reticular hyperpigmentation Wide intermamillary distance Foot oligodactyly Abnormality of the middle ear Rough bone trabeculation Absent toenail Absent fingernail Bladder carcinoma Hypoplastic labia majora Hyperextensible skin Orthostatic hypotension Humerus varus Delayed cranial suture closure Rickets Bilateral ptosis Cardiomyopathy Hypertonia Headache Delayed skeletal maturation Clinodactyly of the 5th finger Redundant skin Severe short stature Hypertrophic cardiomyopathy Pallor Craniosynostosis Short humerus Thin vermilion border Triangular face Renal cyst Microcornea Highly arched eyebrow Pulmonary hypoplasia Wormian bones Coxa vara Small for gestational age Osteolysis Cutis laxa Vertigo Oligodontia Micromelia Synophrys Osteomalacia Acute kidney injury Otitis media Synostosis of joints Abnormality of esophagus physiology Keloids Ureteral obstruction Persistent open anterior fontanelle Limited knee extension Absent tibia Long neck Thick hair Broad clavicles Large iliac wings Abnormality of the pubic bone Capitate-hamate fusion Aplasia/hypoplasia of the humerus Rudimentary to absent tibiae Aplastic clavicle Femoral hernia Exostoses Abnormality of the wrist Soft skin Carotid artery tortuosity Carpal synostosis Abnormality of the skull Atypical scarring of skin Premature skin wrinkling Generalized joint laxity Venous insufficiency Broad ribs Prominent superficial veins Avascular necrosis of the capital femoral epiphysis Abnormality of fibula morphology Aortic rupture Bladder diverticulum Narrow face Dental crowding Aspiration pneumonia Mutism Abnormal pattern of respiration Thickened helices Breathing dysregulation Abnormality of the helix Clubbing of fingers Misalignment of teeth Hyperventilation Hodgkin lymphoma Dysphasia Aphasia Overlapping toe Cupped ear Tricuspid regurgitation Hypopigmented skin patches Aplasia/Hypoplasia of the corpus callosum Happy demeanor Aganglionic megacolon Poor appetite Weak cry Cyanosis Opisthotonus Thick lower lip vermilion Ectopic kidney Pelvic bone exostoses Abnormal palate morphology Truncal ataxia 2-3 toe syndactyly Short middle phalanx of finger Cutis marmorata Abnormal autonomic nervous system physiology Intellectual disability, progressive Pes valgus Large beaked nose Large fontanelles Long eyelashes Joint hyperflexibility Elbow flexion contracture Long face Joint hypermobility Aspiration Bruising susceptibility Choanal atresia Platyspondyly Hypertrichosis Hepatitis Cholestasis High myopia Microdontia Abnormality of the face Narrow chest Torticollis Square face Triangular nasal tip Small cerebral cortex Failure of eruption of permanent teeth Narrow foot Intermittent hyperventilation Proximal placement of thumb Broad fingertip Overhanging nasal tip Pectus carinatum Skeletal muscle atrophy Abnormality of the urinary system Hypoplasia of the radius Renal insufficiency High forehead Jaundice Postnatal microcephaly Type II diabetes mellitus Renal hypoplasia/aplasia Juvenile rheumatoid arthritis Conotruncal defect Velopharyngeal insufficiency Giant platelets Retinal vascular tortuosity Paranoia Duodenal stenosis Impaired T cell function Right aortic arch Mood swings Platybasia Interrupted aortic arch Graves disease Aplasia of the uterus Seborrheic dermatitis Pulmonary artery atresia Arteria lusoria Anal stenosis Abnormality of the ear Basal ganglia calcification Autoimmune hemolytic anemia Axonal loss Submucous cleft hard palate Autoimmune thrombocytopenia Posterior embryotoxon Abnormality of the endocrine system Bipolar affective disorder Vitiligo Hypoparathyroidism Hearing abnormality Meningocele Delusions Aplasia of the thymus Central nervous system degeneration Hypoplasia of the brainstem Nephritis Hemiparesis Exotropia Muscle stiffness Hemivertebrae Neoplasm of the skin Glomerulonephritis Melanocytic nevus Hypotension Disproportionate tall stature Milia Basal cell carcinoma Long fingers Agenesis of permanent teeth Abnormality of the sternum Abnormality of the ribs Nevus Vascular ring Spasticity Perineal fistula Congenital conductive hearing impairment Right aortic arch with mirror image branching Sacral meningocele Unilateral lung agenesis Unilateral primary pulmonary dysgenesis Frontal bossing Palmoplantar keratoderma Kyphoscoliosis EEG abnormality Carcinoma Facial palsy Oral cleft Postaxial polydactyly Myopathic facies Acne Sprengel anomaly Abnormality of the genitourinary system Cutaneous amyloidosis Generalized reticulate brown pigmentation Skeletal dysplasia Feeding difficulties in infancy Bowing of the long bones Joint dislocation Prominent supraorbital ridges Urethral stricture Patent foramen ovale Hyperostosis Hip contracture Tracheal stenosis Neurogenic bladder Fused cervical vertebrae Recurrent infection of the gastrointestinal tract Broad eyebrow Subglottic stenosis Hypohidrosis Visual impairment Gait disturbance Dystonia Abnormality of metabolism/homeostasis Hyperkeratosis Bronchiectasis Recurrent pneumonia Corneal scarring Opacification of the corneal stroma Corneal dystrophy Hemiplegia Keratitis Amyloidosis Focal dystonia Ulnar deviation of the hand Sclerotic vertebral endplates Unilateral renal agenesis Schizophrenia Tetralogy of Fallot Renal dysplasia Hallucinations Hypocalcemia Purpura Holoprosencephaly Abnormality of the hand Renal agenesis Cholelithiasis Dysdiadochokinesis Rheumatoid arthritis Psoriasiform dermatitis Apathy Obsessive-compulsive behavior Peripheral demyelination Underdeveloped nasal alae Large joint dislocations Mental deterioration Cerebellar atrophy Depressivity Dementia Posteriorly rotated ears Hypothyroidism Arthritis Blepharophimosis Chorea Autoimmunity Congenital cataract Anal atresia Dysmetria Bulbous nose Hemolytic anemia Thoracic scoliosis Narrow nose Abnormality of dental enamel Ocular albinism Hypopnea Narrow palm Hypoplastic labia minora Central adrenal insufficiency Temperature instability Triangular mouth Disseminated intravascular coagulation Erysipelas Frontal upsweep of hair Anteverted ears Poor fine motor coordination Abdominal obesity Cor pulmonale Generalized hypopigmentation Chromosome breakage Poor gross motor coordination Pulmonary embolism Truncal obesity External genital hypoplasia Polyphagia Myeloid leukemia Impaired pain sensation Striae distensae Hypopigmentation of hair Hypoplasia of the fovea Hypoventilation Iris hypopigmentation Abnormality of lipid metabolism Central hypotonia Overweight Oligomenorrhea Almond-shaped palpebral fissure Acromicria Skeletal muscle hypertrophy Subcutaneous nodule Overgrowth Postaxial hand polydactyly Interphalangeal joint contracture of finger Split hand Thin skin Omphalocele Hypoplasia of dental enamel Nail dysplasia Telangiectasia Abnormality of epiphysis morphology Short phalanx of finger Hoarse voice Abnormality of the nail Horseshoe kidney Abnormality of the skin Dental malocclusion Alopecia Microtia Agenesis of corpus callosum Reduced visual acuity Erythema Abnormal cardiac septum morphology Camptodactyly of finger Cough Corneal opacity Ectodermal dysplasia Finger syndactyly Nail dystrophy Abnormality of the foot Facial asymmetry Hypodontia Intestinal malrotation Adrenal insufficiency Albinism Fragile nails Cardiac rhabdomyoma Palmar pits Orbital cyst Calcification of falx cerebri Histiocytoma Curved fingers Bifid ribs Odontogenic keratocysts of the jaw Severe hydrocephalus Ovarian fibroma Plantar pits Bridged sella turcica Cardiac fibroma Irregular ossification of hand bones Hamartomatous stomach polyps Short distal phalanx of the thumb Multiple impacted teeth Edema Astrocytoma Skin tags Short 4th metacarpal Abnormality of the neck Neoplasm of the endocrine system Broad face Brain neoplasm Medulloblastoma Ovarian carcinoma Ectopic calcification Cervical ribs Hamartomatous polyposis Fibroma Vertebral wedging Parietal bossing Ventriculomegaly Myopathy Glucose intolerance Aortic valve stenosis Abnormality of the cardiovascular system Oligohydramnios Decreased fetal movement Cutaneous photosensitivity Clumsiness Insulin resistance Scrotal hypoplasia Growth hormone deficiency Infantile muscular hypotonia Precocious puberty Hyperinsulinemia Radial deviation of finger Emotional lability Large hands Febrile seizures Esotropia Congestive heart failure Abnormality of the nervous system Short nose Hyporeflexia Hypogonadism Diabetes mellitus Respiratory failure Neonatal hypotonia Attention deficit hyperactivity disorder Gastrointestinal hemorrhage Stroke Leukemia Hypermetropia Infertility Polymicrogyria Short foot Recurrent abscess formation


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