Hydrocephalus, and Gastrointestinal hemorrhage

Diseases related with Hydrocephalus and Gastrointestinal hemorrhage

In the following list you will find some of the most common rare diseases related to Hydrocephalus and Gastrointestinal hemorrhage that can help you solving undiagnosed cases.

Top matches:

Lymphangioleiomyomatosis (LAM) is a multiple cystic lung disease characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas (AMLs). LAM occurs either sporadically or as a manifestation of tuberous sclerosis complex (TSC).

LYMPHANGIOLEIOMYOMATOSIS Is also known as lam|lymphangiomyomatosis

Related symptoms:

  • Seizures
  • Pain
  • Cognitive impairment
  • Fever
  • Optic atrophy


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about LYMPHANGIOLEIOMYOMATOSIS

Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders (JSRD, see this term) characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF).

JOUBERT SYNDROME WITH HEPATIC DEFECT Is also known as coach syndrome|cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis|cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, ocular coloboma, and hepatic fibrosis|js-h|joubert syndrome with congenital hepatic fibro

Related symptoms:

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


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about JOUBERT SYNDROME WITH HEPATIC DEFECT

Adams-Oliver Syndrome (AOS) is a rare disorder characterized by the combination of congenital limb abnormalities and scalp defects, often accompanied by skull ossification defects.

ADAMS-OLIVER SYNDROME Is also known as aplasia cutis congenita with terminal transverse limb defects|congenital scalp defects with distal limb reduction anomalies|congenital scalp defects with distal limb anomalies|aos|absence defect of limbs, scalp, and skull|limb, scalp and skull defects

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about ADAMS-OLIVER SYNDROME

Other less relevant matches:

Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.

EHLERS-DANLOS SYNDROME, VASCULAR TYPE Is also known as ehlers-danlos syndrome, type iv, autosomal dominant|eds type 4|ehlers-danlos syndrome type 4|ehlers-danlos syndrome type iv|ehlers-danlos syndrome, ecchymotic type|ehlers-danlos syndrome, arterial type|eds4|sack-barabas syndrome|eds iv|ehlers-danlos syndr

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hypertelorism
  • Pain
  • Cryptorchidism


SOURCES: ORPHANET OMIM MENDELIAN

More info about EHLERS-DANLOS SYNDROME, VASCULAR TYPE

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

22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.

22Q11.2 DELETION SYNDROME Is also known as monosomy 22q11|digeorge sequence|sedlackova syndrome|takao syndrome|velocardiofacial syndrome|shprintzen syndrome|conotruncal anomaly face syndrome|digeorge syndrome|catch 22|cayler cardiofacial syndrome|microdeletion 22q11.2|22q11ds

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET MENDELIAN

More info about 22Q11.2 DELETION SYNDROME

Costello syndrome (CS) is a rare multisystemic disorder characterized by failure to thrive, short stature, developmental delay or intellectual disability, joint laxity, soft skin, and distinctive facial features. Cardiac and neurological involvement is common and there is an increased lifetime risk of certain tumors.

COSTELLO SYNDROME Is also known as fcs syndrome|faciocutaneoskeletal syndrome

Related symptoms:

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


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about COSTELLO SYNDROME

Deficiency of all vitamin K-dependent clotting factors leads to a bleeding tendency that is usually reversed by oral administration of vitamin K. Familial multiple coagulation factor deficiency is rare. Clinical symptoms of the disease include episodes of intracranial hemorrhage in the first weeks of life, sometimes leading to a fatal outcome (Fregin et al., 2002).

Related symptoms:

  • Hydrocephalus
  • Abnormal bleeding
  • Intracranial hemorrhage
  • Reduced factor IX activity
  • Reduced factor VII activity


SOURCES: MESH OMIM MENDELIAN

More info about VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2

Congenital hydrocephalus-1 is characterized by onset in utero of enlarged ventricles due to a disturbance of cerebrospinal fluid accumulation. Affected individuals may have neurologic impairment (summary by Drielsma et al., 2012).Hydrocephalus can also be caused by Arnold-Chiari malformation, atresia of foramen of Magendie, stenosis of aqueduct of Sylvius (OMIM ), toxoplasmosis, hydranencephaly, etc. Furthermore, it develops in infancy or childhood in achondroplasia (OMIM ) and in Hurler disease (OMIM ). Genetic Heterogeneity of Congenital HydrocephalusSee also HYC2 (OMIM ), caused by mutation in the MPDZ gene (OMIM ) on chromosome 9p23, and HYC3 (OMIM ), caused by mutation in the WDR81 gene (OMIM ) on chromosome 17p13.An X-linked form of congenital hydrocephalus (HSAS, HYCX; {307000}) is caused by mutation in the L1CAM gene on (OMIM ) on chromosome Xq28.

HYDROCEPHALUS, CONGENITAL, 1; HYC1 Is also known as hydrocephaly|hydrocephalus, nonsyndromic, autosomal recessive 1, formerly|ventriculomegaly

Related symptoms:

  • Intellectual disability
  • Seizures
  • Neoplasm
  • Macrocephaly
  • Ventriculomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about HYDROCEPHALUS, CONGENITAL, 1; HYC1

Focal facial dermal dysplasia type IV (FFDD4) is a rare focal facial dysplasia (FFDD; see this term), characterized by congenital isolated preauricular and/or cheek blister scar-like lesions.

FOCAL FACIAL DERMAL DYSPLASIA TYPE IV Is also known as ffdd type iv|focal facial dermal dysplasia 4|focal facial preauricular dysplasia|ffdd4

Related symptoms:

  • Microcephaly
  • Cleft palate
  • Hydrocephalus
  • Cleft lip
  • Sparse hair


SOURCES: OMIM ORPHANET MENDELIAN

More info about FOCAL FACIAL DERMAL DYSPLASIA TYPE IV

Top 5 symptoms//phenotypes associated to Hydrocephalus and Gastrointestinal hemorrhage

Symptoms // Phenotype % cases
Seizures Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Abnormality of cardiovascular system morphology Uncommon - Between 30% and 50% cases
Dilatation Uncommon - Between 30% and 50% cases
Macrocephaly Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Hydrocephalus and Gastrointestinal hemorrhage. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Ptosis Hypertelorism Global developmental delay Hypertension Cognitive impairment Inguinal hernia Scoliosis Short stature Strabismus Muscular hypotonia Talipes equinovarus Cryptorchidism Neoplasm Generalized hypotonia Abnormal pulmonary valve morphology Growth delay Prominent nasal bridge Low-set ears Premature birth Epicanthus Short chin Mitral valve prolapse Feeding difficulties in infancy Downslanted palpebral fissures Respiratory insufficiency Abnormality of the dentition Joint hyperflexibility Carious teeth Glaucoma Abnormal facial shape Microcephaly Tetralogy of Fallot Atrial septal defect Pain Ventricular septal defect Abnormality of the skeletal system Abnormal heart morphology Osteopenia Sparse hair Pneumothorax Intellectual disability, mild Ascites Cleft palate Abnormality of skin pigmentation Failure to thrive Pulmonic stenosis Ventriculomegaly

Rare Symptoms - Less than 30% cases

Hypospadias Pectus excavatum Cataract Intrauterine growth retardation Narrow mouth Polymicrogyria Cutis laxa Microphthalmia Cleft upper lip Patent ductus arteriosus Alopecia Arnold-Chiari malformation Central hypotonia Aplasia cutis congenita Telangiectasia Hemiparesis Coarctation of aorta Proptosis Leukemia Thrombocytopenia Long philtrum Umbilical hernia Hypertrophic cardiomyopathy Blindness Behavioral abnormality Headache Depressivity Osteoporosis Autism Kyphoscoliosis Hypoglycemia Attention deficit hyperactivity disorder Dysarthria Specific learning disability Overgrowth Aganglionic megacolon Cafe-au-lait spot Laryngomalacia Short neck Spina bifida Abnormality of dental enamel Gastroesophageal reflux Cardiomyopathy Delayed speech and language development Arthritis Nevus Embryonal rhabdomyosarcoma Telecanthus Joint hypermobility High, narrow palate Abnormal bleeding Polyhydramnios Vestibular Schwannoma Congenital hepatic fibrosis Schwannoma Normal pressure hydrocephalus Redundant skin Aortic aneurysm Rhabdomyosarcoma Keratoconus Micrognathia Aqueductal stenosis Irritability Varicose veins Renovascular hypertension Abnormality of the skin Hemangioma Esophageal varix Splenomegaly Respiratory failure Cirrhosis Cerebellar hypoplasia Renal insufficiency Encephalocele Visual impairment Lymphedema Apraxia Long face Intellectual disability, severe Intestinal malrotation Intracranial hemorrhage Anteverted nares Atelectasis Hepatomegaly Hematuria Nystagmus Frontal bossing Portal hypertension Chylothorax Abnormality of the nervous system Intellectual disability, moderate Apnea Abnormality of the kidney Optic atrophy Wide mouth Multiple renal cysts Macule Hemoptysis Reduced factor X activity Prominent forehead Abnormality of the uterus Chronic obstructive pulmonary disease Vomiting Turricephaly Abnormal eyelid morphology Truncus arteriosus Reduced factor IX activity Meningocele Reduced prothrombin activity Abnormality of the skull Hypoparathyroidism Corneal neovascularization Reduced factor VII activity Patellar dislocation Abnormal aortic valve morphology Tetany Cerebral atrophy Motor delay Myopia Dysphagia Edema Myopathy Short nose Absent speech Feeding difficulties Hernia Arrhythmia Systolic heart murmur Delayed skeletal maturation Pes cavus Severe short stature Depressed nasal bridge High palate Hypoplasia of the thymus Arrhinencephaly Seborrheic dermatitis Abnormal thrombocyte morphology Abnormality of the pharynx Small earlobe Platybasia Increased corneal curvature Impaired T cell function Occipital myelomeningocele Anorectal anomaly Retinal arteriolar tortuosity Hypertensive crisis Abnormal aortic arch morphology Multiple suture craniosynostosis Tricuspid atresia Abnormality of the tonsils Mental deterioration Communicating hydrocephalus Stroke Constipation Wide nasal bridge Unilateral cleft lip Skin vesicle Malar flattening Immunodeficiency Obesity Upslanted palpebral fissure Hearing impairment Hypothyroidism Cupped ear Dermal atrophy Conductive hearing impairment Myalgia Anxiety Abnormality of the cheek Brow ptosis Short philtrum Acute promyelocytic leukemia Axillary freckling Abnormality of buccal mucosa Neuroma Neurofibrosarcoma Optic nerve glioma Subcutaneous neurofibromas Plexiform neurofibroma Tibial pseudoarthrosis Abnormal mast cell morphology Inguinal freckling Spinal neurofibromas Fragmented elastic fibers in the dermis Arterial fibromuscular dysplasia Cerebral artery stenosis Autoimmunity Anal atresia Bipolar affective disorder Hyperthyroidism Abnormality of the thorax Overfolded helix Chronic otitis media Acne Dysphasia Bowel incontinence Hydranencephaly Intraventricular hemorrhage Dilated fourth ventricle Foot polydactyly Hyperhidrosis Posterior embryotoxon Abnormal lung lobation Spontaneous abortion Hand polydactyly Cleft lip Arachnodactyly Purpura Bulbous nose Asthma Vesicoureteral reflux Renal hypoplasia Choanal atresia Hypocalcemia Hypopigmented skin patches Cholelithiasis Schizophrenia Abnormal blistering of the skin Focal-onset seizure Nasal speech Scarring Polycystic kidney dysplasia Posteriorly rotated ears Congenital neuroblastoma Hypogonadism Microscopic hematuria Achilles tendon contracture Concentric hypertrophic cardiomyopathy Thick upper lip vermilion Large earlobe Transitional cell carcinoma of the bladder Ganglioneuroblastoma Woolly hair Progeroid facial appearance Frontal hirsutism Barrel-shaped chest Megalencephaly Deep-set nails Fragile nails Thickened nuchal skin fold Severe postnatal growth retardation Large forehead Obstructive sleep apnea Soft skin Neonatal hypoglycemia Arnold-Chiari type I malformation Syringomyelia Tracheomalacia Generalized hyperpigmentation Ulnar deviation of finger Rhabdomyolysis Neuroblastoma Curly hair Reduced subcutaneous adipose tissue Neurodevelopmental delay Large for gestational age Hypopnea Verrucae Tricuspid regurgitation Deep plantar creases Hyperextensibility of the finger joints Abnormality of earlobe Concave nail Hypoplasia of teeth Fasting hypoglycemia Broad philtrum Abnormal mitral valve morphology Limited elbow movement Fetal distress Bronchomalacia Papilloma Asymmetric septal hypertrophy Large face Thin nail Hematemesis Shyness Melena Deep palmar crease Labial hypoplasia Redundant neck skin Triangular mouth Capillary malformation Bladder neoplasm Duodenal ulcer Ulnar deviation of the wrist Body odor Abnormality of the testis Postprandial hyperglycemia Lack of skin elasticity Central apnea Rocker bottom foot Hypoplastic toenails Cerebral cortical atrophy Thick vermilion border Thick lower lip vermilion Epidermal acanthosis Eczema Hip dysplasia Growth hormone deficiency Alveolar rhabdomyosarcoma Webbed neck Full cheeks Sepsis Macroglossia Tetraplegia Lymphangiectasis Postural instability Sleep disturbance Wide nose Hypoplasia of dental enamel Tachycardia Astigmatism Delayed puberty Hypermetropia Arthrogryposis multiplex congenita Broad femoral neck Pectus carinatum Postnatal growth retardation Thickened Achilles tendon Low-set, posteriorly rotated ears Joint laxity Carcinoma Coarse facial features Hyperkeratosis Atrial fibrillation Decreased body weight Bilateral cryptorchidism Bladder carcinoma Hyperglycemia Heart murmur Pleural effusion Failure to thrive in infancy Pyloric stenosis Multifocal atrial tachycardia Hyperextensible skin Poor suck Relative macrocephaly Neonatal sepsis Single ventricle Infantile muscular hypotonia Abnormal dermatoglyphics Choroid plexus papilloma Cardiomyocyte hypertrophy Long eyelashes Hoarse voice Hyperpigmentation of the skin Tendon rupture Wide anterior fontanel Vitreomacular adhesion Hydrops fetalis Abnormality of the hair Pointed chin Loose anagen hair Narrow palate Abnormality of the fingernails Acanthosis nigricans Myofiber disarray Enlarged cerebellum Macrocephaly at birth Renal artery stenosis Paralysis Pseudoarthrosis Nail dysplasia Aplasia/Hypoplasia of the skin Cortical dysplasia Hypoplastic left heart Supernumerary nipple Cutis marmorata Abnormality of the metacarpal bones Bicuspid aortic valve Leukopenia Meningitis Aortic valve stenosis Pachygyria Split hand Small nail Pulmonary arterial hypertension Esotropia Oligodactyly Short distal phalanx of finger Talipes Toe syndactyly Finger syndactyly Abnormal cardiac septum morphology EEG abnormality Syndactyly Hypertonia Hypoplasia of the corpus callosum Brachydactyly Intrahepatic biliary atresia Chronic hepatic failure Multiple small medullary renal cysts Aplasia/Hypoplasia of the cerebellar vermis Cutaneous finger syndactyly Pulmonary artery stenosis Abnormality of the hypothalamus-pituitary axis Imperforate hymen Blue sclerae Microdontia Migraine Bruising susceptibility Flat face Thin vermilion border Vertigo Hip dislocation Protruding ear Deeply set eye Flexion contracture Aplasia cutis congenita on trunk or limbs Aplasia cutis congenita over posterior parietal area Acrania Periventricular cysts Double outlet right ventricle Porencephalic cyst Calvarial skull defect Arteriovenous malformation Abnormality of the lower limb Hypoplastic fingernail Pulmonary artery atresia Abnormality of the upper limb Periventricular leukomalacia Cutis marmorata telangiectatica congenita Aplasia cutis congenita of scalp Aplastic/hypoplastic toenail Absent hand Absent fingernail Venous malformation Absent toe Abnormal pattern of respiration Cholestatic liver disease Thin skin Renal neoplasm Spasticity Ataxia Chylopericardium Pulmonary lymphangiomyomatosis Cystic lung disease Ungual fibroma Retinal hamartoma Renal angiomyolipoma Bronchiolitis obliterans Shagreen patch Abnormal urinary color Abnormality of the lymphatic system Bronchiolitis Abnormality of female internal genitalia Pulmonary infiltrates Tremor Cough Fever Fatigue Respiratory distress Recurrent respiratory infections Abdominal pain Dyspnea Lymphadenopathy Restrictive ventilatory defect Chest pain Myocardial infarction Abnormal lung morphology Melanoma Nephroblastoma Emphysema Hyperreflexia Gait disturbance Neoplasm of the liver Cholestasis Optic nerve coloboma Abnormality of abdomen morphology Biparietal narrowing Occipital encephalocele Nephronophthisis Molar tooth sign on MRI Abnormality of neuronal migration Aplasia/Hypoplasia of the cerebellum Chorioretinal coloboma Chronic kidney disease Aplasia/Hypoplasia of the corpus callosum Oculomotor apraxia Multicystic kidney dysplasia Hepatic fibrosis Cerebellar vermis hypoplasia Agenesis of corpus callosum Oral cleft Polydactyly Elevated hepatic transaminase Abnormality of the eye Abnormality of the liver Coloboma Abnormality of eye movement Stage 5 chronic kidney disease Postaxial hand polydactyly Iris coloboma Retinal dystrophy Nephropathy Highly arched eyebrow Renal cyst Round face Osteoarthritis Abnormality of the face Soft tissue sarcoma Lymphoma Sensory axonal neuropathy Clitoral hypertrophy Precocious puberty Back pain Sarcoma Incoordination Breast carcinoma Reduced bone mineral density Venous thrombosis Atherosclerosis Sensorimotor neuropathy Bone pain Hypsarrhythmia Abnormality of the cardiovascular system Recurrent fractures Pulmonary fibrosis Hyperactivity Premature delivery because of cervical insufficiency or membrane fragility Hemothorax Hypermobility of distal interphalangeal joints Anemia Peripheral neuropathy Visual loss Weight loss Peripheral axonal neuropathy Autistic behavior Pruritus Malabsorption Genu valgum Facial asymmetry Paresthesia Hypophosphatemia Neurofibromas Hypoplastic lacrimal duct Anomalous pulmonary venous return Epigastric pain Dural ectasia Leiomyosarcoma Fibular bowing Gastrointestinal stroma tumor Neoplasm of the central nervous system Lisch nodules Chronic myelogenous leukemia Renal phosphate wasting Glioma Nasolacrimal duct obstruction Carcinoid tumor Paraganglioma Night sweats Complete atrioventricular canal defect Tibial bowing Increased reactive oxygen species production Freckling Multiple cafe-au-lait spots Osteomalacia Renal cell carcinoma Severe vision loss Overweight Gangrene Pheochromocytoma Meningioma Neoplasm of the endocrine system Myocardial fibrosis Brain neoplasm Astrocytoma Parathyroid adenoma Cystocele Arteriovenous fistulas of celiac and mesenteric vessels Subcutaneous nodule Fragile skin Aortic dissection Gingivitis Transient ischemic attack Narrow nose Abnormal eyelash morphology Subarachnoid hemorrhage Dilatation of the cerebral artery Alopecia of scalp Premature loss of teeth Sprengel anomaly Esophageal atresia Prematurely aged appearance Scleroderma Abnormal joint morphology Abnormal heart valve morphology Abnormally large globe Sleep apnea Gingival overgrowth Cardiac arrest Congenital hip dislocation Joint dislocation Osteolysis Abnormal intestine morphology Tinnitus Telangiectasia of the skin Abnormality of the urinary system Hypokalemia Rheumatoid arthritis Melanocytic nevus Aplasia/Hypoplasia of the eyebrow Narrow nasal bridge Periodontitis Hematochezia Uterine prolapse Colonic diverticula Uterine rupture Arterial rupture Foot acroosteolysis Spontaneous pneumothorax Molluscoid pseudotumors Coronary artery aneurysm Gingival recession Pulmonary artery aneurysm Peripheral arteriovenous fistula Absent earlobe Arteriovenous fistula Cigarette-paper scars Arterial dissection Internal hemorrhage Abnormality of the gingiva Osteolytic defects of the phalanges of the hand Premature loss of primary teeth Reduced consciousness/confusion Aplasia/Hypoplasia of the earlobes Abnormal pupil morphology Aplasia/Hypoplasia of the abdominal wall musculature Bladder diverticulum Periorbital edema Arterial stenosis Abnormal oral frenulum morphology Ocular pain Abnormality of hair texture Excessive wrinkled skin Ascending tubular aorta aneurysm Dermal translucency Gastrointestinal infarctions Abnormality of epidermal morphology


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