Leukemia, and Dolichocephaly

Diseases related with Leukemia and Dolichocephaly

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

Top matches:

Noonan syndrome is an autosomal dominant dysmorphic syndrome characterized primarily by dysmorphic facial features, cardiac abnormalities, and short stature, among other features (summary by Shah et al., 1999).For a phenotypic description and a discussion of genetic heterogeneity of Noonan syndrome, see NS1 (OMIM ), which is caused by mutations in the PTPN11 gene (OMIM ). Approximately 50% of cases of Noonan syndrome are caused by mutations in PTPN11.

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hypertelorism
  • Strabismus
  • Abnormal facial shape


SOURCES: OMIM MESH MENDELIAN

More info about NOONAN SYNDROME 3; NS3

Medium match MEVALONIC ACIDURIA

Mevalonic aciduria (MVA) is a rare, very severe form of mevalonate kinase deficiency (MKD; see this term) characterized by dysmorphic features, failure to thrive, psychomotor delay, ocular involvement, hypotonia, progressive ataxia, myopathy, and recurrent inflammatory episodes.

MEVALONIC ACIDURIA Is also known as mva|complete mevalonate kinase deficiency

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about MEVALONIC ACIDURIA

Medium match BLOOM SYNDROME

Bloom syndrome (BSyn) is a rare chromosomal breakage syndrome characterized by a marked genetic instability associated with pre- and postnatal growth retardation, facial sun-sensitive telangiectatic erythema, increased susceptibility to infections, and predisposition to cancer.

BLOOM SYNDROME Is also known as bls|microcephaly, growth restriction, and increased sister chromatid exchange 1|bs|bsyn|mgrisce1

Related symptoms:

  • Short stature
  • Microcephaly
  • Growth delay
  • Neoplasm
  • Failure to thrive


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about BLOOM SYNDROME

Other less relevant matches:

Mosaic variegated aneuploidy (MVA) syndrome is a chromosomal anomaly characterized by multiple mosaic aneuploidies that leads to a variety of phenotypic abnormalities and cancer predisposition.

MOSAIC VARIEGATED ANEUPLOIDY SYNDROME Is also known as warburton-anyane-yeboa syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about MOSAIC VARIEGATED ANEUPLOIDY SYNDROME

SOTOS SYNDROME 1; SOTOS1 Is also known as chromosome 5q35 deletion syndrome|sotos syndrome|cerebral gigantism

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about SOTOS SYNDROME 1; SOTOS1

Low match COWDEN SYNDROME

Cowden syndrome (CS) is a difficult to recognize, under-diagnosed genodermatosis characterized by the presence of multiple hamartomas in various tissues and an increased risk for malignancies of the breast, thyroid, endometrium, kidney and colorectum. When CS is accompanied by germline PTEN mutations, it belongs to the PTEN hamartoma tumor syndrome (PHTS; see this term) group.

COWDEN SYNDROME Is also known as bzs|cowden disease|bbrs|macrocephaly, multiple lipomas, and hemangiomata|pten hamartoma tumor syndrome with granular cell tumor|bannayan-zonana syndrome|macrocephaly, pseudopapilledema, and multiple hemangiomata|cs|cd|mham|pten hamartoma tumor syndrome|ri

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about COWDEN SYNDROME

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

Low match FANCONI ANEMIA

Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.

FANCONI ANEMIA Is also known as fanconi pancytopenia|fanconi anemia|fa

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about FANCONI ANEMIA

Cardiofaciocutaneous (CFC) syndrome is a RASopathy characterized by craniofacial dysmorphology, congenital heart disease, dermatological abnormalities (most commonly hyperkeratotic skin and sparse, curly hair), growth retardation and intellectual disability.

CARDIOFACIOCUTANEOUS SYNDROME Is also known as cfcs|cfc syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about CARDIOFACIOCUTANEOUS SYNDROME

Jacobsen syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11.

JACOBSEN SYNDROME Is also known as monosomy 11qter|del(11)(q23.3)|distal deletion 11q|telomeric deletion 11q|distal monosomy 11q|del(11)(qter)|chromosome 11q deletion syndrome|partial 11q monosomy syndrome

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about JACOBSEN SYNDROME

Top 5 symptoms//phenotypes associated to Leukemia and Dolichocephaly

Symptoms // Phenotype % cases
Global developmental delay Very Common - Between 80% and 100% cases
Short stature Very Common - Between 80% and 100% cases
Intellectual disability Common - Between 50% and 80% cases
Atrial septal defect Common - Between 50% and 80% cases
Neoplasm Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Leukemia and Dolichocephaly. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases

Frontal bossing

Uncommon Symptoms - Between 30% and 50% cases

Downslanted palpebral fissures

Common Symptoms - More than 50% cases

Generalized hypotonia

Uncommon Symptoms - Between 30% and 50% cases

Micrognathia

Common Symptoms - More than 50% cases

Seizures

Uncommon Symptoms - Between 30% and 50% cases

Abnormal facial shape

Common Symptoms - More than 50% cases

Failure to thrive

Uncommon Symptoms - Between 30% and 50% cases

Ventriculomegaly

Common Symptoms - More than 50% cases

Scoliosis

Uncommon Symptoms - Between 30% and 50% cases

Hearing impairment

Common Symptoms - More than 50% cases

Cryptorchidism

Uncommon Symptoms - Between 30% and 50% cases

Growth delay

Common Symptoms - More than 50% cases

Short nose

Uncommon Symptoms - Between 30% and 50% cases

Hypertelorism

Common Symptoms - More than 50% cases

Strabismus

Uncommon Symptoms - Between 30% and 50% cases

Low-set ears

Common Symptoms - More than 50% cases

High palate

Uncommon Symptoms - Between 30% and 50% cases

Cataract

Common Symptoms - More than 50% cases

Epicanthus

Uncommon Symptoms - Between 30% and 50% cases

Microcephaly Abnormal heart morphology Macrocephaly Ventricular septal defect Nystagmus Cafe-au-lait spot Clinodactyly of the 5th finger Intellectual disability, mild Intrauterine growth retardation Muscular hypotonia Low-set, posteriorly rotated ears Hypothyroidism Abnormality of the dentition Depressed nasal bridge Abnormality of cardiovascular system morphology Thrombocytopenia Growth hormone deficiency Multiple cafe-au-lait spots Delayed speech and language development Behavioral abnormality Prominent forehead Hydrocephalus Congestive heart failure Delayed skeletal maturation Abnormality of the kidney Optic atrophy Cognitive impairment Patent ductus arteriosus Pectus excavatum Ptosis Ataxia Myopia Telangiectasia Clinodactyly Microphthalmia Chromosome breakage Acute myeloid leukemia Myeloid leukemia Hand polydactyly Hypopigmented skin patches Azoospermia Otitis media High forehead Decreased antibody level in blood Lymphoma Finger syndactyly Postnatal growth retardation Diabetes mellitus Recurrent respiratory infections Recurrent infections Immunodeficiency Syndactyly Webbed neck Abnormality of the eye Edema Kyphosis Feeding difficulties Joint hypermobility Genu valgum Hypermetropia Respiratory tract infection Anteverted nares Carcinoma Pes planus Hypogonadism Autism Small for gestational age Posteriorly rotated ears Polyhydramnios Osteopenia Hypertrophic cardiomyopathy Abnormality of vision Sleep apnea Coarctation of aorta Pain Abnormality of skin pigmentation Sloping forehead Craniosynostosis Anemia Myopathy Diarrhea Vomiting Fever Hepatomegaly Bruising susceptibility Skin rash Abnormal cardiac septum morphology Hypoglycemia Cerebral atrophy Clumsiness

Rare Symptoms - Less than 30% cases

Intestinal polyposis Subvalvular aortic stenosis Nephroblastoma Brachydactyly Attention deficit hyperactivity disorder Abnormality of the liver Atrioventricular canal defect Abnormality of the upper limb Motor delay Feeding difficulties in infancy Acute lymphoblastic leukemia Telecanthus Thin upper lip vermilion Duodenal atresia Myelodysplasia Anal atresia Long philtrum Retinal dystrophy Long face Bulbous nose Sleep disturbance Narrow mouth Dilatation Weight loss Facial asymmetry Short palpebral fissure Headache Hypospadias Multicystic kidney dysplasia Holoprosencephaly Pruritus Aplasia/Hypoplasia of the corpus callosum Abnormality of the nervous system Abnormal aortic morphology Narrow palate Overgrowth Talipes equinovarus Constipation Hamartomatous polyposis Lymphedema Abnormal vertebral morphology Inguinal hernia Abnormal eyelash morphology Vesicoureteral reflux Cutis laxa Redundant skin Precocious puberty Large hands Partial agenesis of the corpus callosum Splenomegaly Hernia Renal agenesis Intellectual disability, severe Increased nuchal translucency Irritability Hydronephrosis Intellectual disability, moderate Toe syndactyly Hyperreflexia Hip dislocation Macrotia Coarse facial features Upslanted palpebral fissure High, narrow palate Neonatal hypotonia Osteoporosis Umbilical hernia Aggressive behavior Cerebral cortical atrophy Proptosis Almond-shaped palpebral fissure Obesity Astigmatism Hypopigmentation of the skin Full cheeks Nuclear cataract Intestinal malrotation Specific learning disability Type II diabetes mellitus Cutaneous photosensitivity Hyperinsulinemia Failure to thrive in infancy Scaphocephaly Premature birth Sinusitis Narrow face Hemangioma Triangular face Cranial nerve paralysis Reduced number of teeth Pancytopenia Abnormality of the uterus Palmoplantar hyperkeratosis Poor suck Severe short stature Cardiomyopathy Hydroureter Malar flattening Abnormal palate morphology Horseshoe kidney Melanocytic nevus Bone marrow hypocellularity Hyperhidrosis Short thumb Hypoplastic anemia Arteriovenous malformation Glucose intolerance Erythema Spina bifida Infertility Ichthyosis Squamous cell carcinoma Short neck Infantile muscular hypotonia Oligohydramnios Apnea Neurological speech impairment Clitoral hypoplasia Pulmonic stenosis Nevus Polymicrogyria Palmoplantar keratoderma Deep philtrum Abnormality of the skeletal system Aplasia/Hypoplasia of the eyebrow Cleft palate Cystic hygroma Abnormality of the cardiovascular system Narrow forehead Abnormal aortic valve morphology Abnormality of chromosome stability Aortic valve stenosis Cavernous hemangioma Hypoplasia of the zygomatic bone Heart murmur Abnormality of the testis Hodgkin lymphoma Abnormality of the ulna Insulin resistance Ectropion Low posterior hairline EEG abnormality Fine hair Myocardial infarction Depressivity Thick vermilion border Hemiparesis Encephalopathy Cardiomegaly Inflammatory abnormality of the skin Nail dystrophy Abdominal distention Progressive visual loss Pectus carinatum Dry skin Alopecia Dental malocclusion Falls Hepatic steatosis Peripheral axonal neuropathy Scarring Sparse hair Hyperkeratosis Abnormal bleeding Abnormality of the cerebral white matter Hypotrichosis Gastroesophageal reflux Abnormality of the urinary system Hypertonia Aganglionic megacolon Acute monocytic leukemia Abnormality of femur morphology Bicornuate uterus Abnormality of the thumb Neutropenia Aplastic anemia B-cell lymphoma Tetralogy of Fallot Abnormal eyelid morphology Choanal atresia Hearing abnormality Abnormality of the genital system External ear malformation Irregular hyperpigmentation Abnormal renal morphology Aplasia/Hypoplasia of the radius Recurrent urinary tract infections Hypergonadotropic hypogonadism Absent radius Abnormality of blood and blood-forming tissues Absent thumb Type I diabetes mellitus Leukopenia Ectopic kidney Hypoplasia of the ulna Tracheoesophageal fistula Triphalangeal thumb Renal hypoplasia/aplasia Abnormality of the hypothalamus-pituitary axis Abnormal localization of kidney Blindness Absent testis Dysphagia Dysarthria Abnormality of the preputium Pyridoxine-responsive sideroblastic anemia Aplasia/Hypoplasia of fingers Aplasia/Hypoplasia of the uvula Neoplasm of head and neck Deficient excision of UV-induced pyrimidine dimers in DNA Anemic pallor Prolonged G2 phase of cell cycle Abnormal carotid artery morphology Compensated hypothyroidism Reduced bone mineral density Chromosomal breakage induced by crosslinking agents Vertigo Decreased fertility in males Abnormality of the foot Clubbing of toes Partial duplication of thumb phalanx Complete duplication of thumb phalanx Aplasia/Hypoplasia of the iris Low-grade fever Meckel diverticulum Duplicated collecting system Decreased body weight Duodenal stenosis Primary hypothyroidism Abnormality of nervous system morphology Reticulocytopenia Open mouth Dystrophic fingernails Thickened skin Microdontia Smooth philtrum Tachycardia Iris coloboma Single transverse palmar crease Microcornea Postural instability Dehydration Narrow chest Eczema Abnormal form of the vertebral bodies Pachygyria Amblyopia Short toe Leukodystrophy Tachypnea Talipes Coloboma Bilateral camptodactyly Megakaryocyte dysplasia Morphological abnormality of the gastrointestinal tract Cutaneous T-cell lymphoma Inappropriate crying Abnormality of the auditory canal Multiple palmar creases Eyelid fasciculation Multiple plantar creases Congenital thrombocytopenia Camptodactyly Oral aversion Sensorineural hearing impairment Spasticity Flexion contracture Wide nasal bridge Agenesis of corpus callosum Retrognathia Schizophrenia Arteria lusoria Abnormal location of ears Broad columella Ectopic anus Mitral stenosis Broad hallux phalanx Aplasia/Hypoplasia of the earlobes Labial hypoplasia Abnormal thrombocyte morphology Nasolacrimal duct obstruction Chronic constipation Abnormality of the head Long hallux Urethral stenosis U-Shaped upper lip vermilion Central hypothyroidism Macular hypoplasia Giant platelets Eyelid coloboma Retinal dysplasia Internal hemorrhage Flat occiput Annular pancreas Abnormality of the anus Toe clinodactyly Pyloric stenosis Trigonocephaly Chorioretinal coloboma Hammertoe Hypoplastic left heart Diastasis recti Slender finger Natal tooth Transposition of the great arteries Wheezing Bipolar affective disorder Double outlet right ventricle Missing ribs Puberty and gonadal disorders Abnormality of the hairline Hyperpigmentation of the skin Long palpebral fissure Open bite Malnutrition Neurodevelopmental delay Neurofibromas Infantile spasms Abnormality of the sternum Abnormal heart valve morphology Absent eyebrow Biparietal narrowing Curly hair Generalized hyperpigmentation Submucous cleft hard palate Anal stenosis Underdeveloped supraorbital ridges Poor appetite Large for gestational age Obsessive-compulsive behavior Alopecia of scalp Optic nerve hypoplasia Cerebral visual impairment Aspiration Abnormality of the nail Sparse eyelashes Oculomotor apraxia Abnormality of the genitourinary system Delayed gross motor development Relative macrocephaly Chronic otitis media Hyperextensible skin Brittle hair Bilateral ptosis Sparse eyebrow Scaling skin Pleural effusion Cubitus valgus Atopic dermatitis Arnold-Chiari type I malformation Hyperkeratosis pilaris Abnormality of the optic disc Abnormality of hair texture Multiple lentigines Sparse or absent eyelashes Endocarditis Frontal balding Anterior creases of earlobe Abnormal tricuspid valve morphology Abnormality of the pulmonary artery Patchy alopecia Optic nerve dysplasia Hypoplasia of the frontal lobes Generalized ichthyosis Laryngeal cleft Functional abnormality of the gastrointestinal tract Tongue thrusting Excessive wrinkled skin Hyperextensibility of the finger joints Enlarged kidney Abnormality of the optic nerve Absent eyelashes Premature skin wrinkling Abnormality of the gastrointestinal tract Short attention span Woolly hair Thick upper lip vermilion Abnormal hair pattern Delayed CNS myelination Respiratory distress Abnormal myocardium morphology Abnormality of refraction Deep palmar crease Gastrointestinal dysmotility Abnormal mitral valve morphology Slow-growing hair Thickened helices Renal insufficiency Trichilemmoma Fatigue Stomach cancer Pointed chin Tall stature Hypoplasia of dental enamel Heterotopia Small nail Apraxia Hypodontia Joint laxity Conductive hearing impairment Jaundice Mandibular prognathia Vaginal neoplasm Premature chromatid separation Epidermoid cyst Rhabdomyosarcoma Abnormal dermatoglyphics Finger clinodactyly Wide nose Ascites Dandy-Walker malformation Ambiguous genitalia Depressed nasal ridge Rhizomelia Osteolysis Abnormality of the skull Microretrognathia Aortic regurgitation Aplasia/Hypoplasia of the cerebellum Colon cancer Abnormality of immune system physiology Abnormal lung lobation Accelerated skeletal maturation Agenesis of permanent teeth Corneal opacity Hypoplasia of the maxilla Muscle weakness Skeletal muscle atrophy Tremor Proximal muscle weakness Papule Nausea and vomiting Abnormal cerebellum morphology Small cell lung carcinoma Macroglossia Intention tremor Broad thumb Subcutaneous nodule Chronic diarrhea Exotropia Abnormality of the cerebral ventricles Gray matter heterotopias Prolonged neonatal jaundice Cavum septum pellucidum Neuroblastoma Poor coordination High anterior hairline Enlarged cisterna magna Long foot Advanced eruption of teeth Oxycephaly Sacrococcygeal teratoma Periventricular leukomalacia Abnormal glucose tolerance Overbite Teratoma Hyperplasia of the maxilla Expressive language delay Muscular dystrophy Blepharophimosis Lymphopenia Large fontanelles Lactic acidosis Metabolic acidosis Progressive cerebellar ataxia Aciduria Underdeveloped nasal alae Blue sclerae Leukocytosis Malabsorption Petechiae Severe failure to thrive Organic aciduria Cholestatic liver disease Agenesis of cerebellar vermis Extramedullary hematopoiesis Lymphadenopathy Elevated hepatic transaminase Glutathione synthetase deficiency Atrial septal dilatation Mitral valve prolapse Pterygium Sagittal craniosynostosis Myeloproliferative disorder Hypoplastic nasal bridge Juvenile myelomonocytic leukemia Dysplastic pulmonary valve Hepatosplenomegaly Cerebellar atrophy Elevated serum creatine phosphokinase Abdominal pain Acidosis Kyphoscoliosis Arthralgia Normocytic anemia Therapeutic abortion Deeply set eye Decreased fertility in females Acute leukemia Hypoplastic pelvis Chronic lung disease Chronic obstructive pulmonary disease Abnormality of the nose IgM deficiency Female infertility IgA deficiency Spotty hypopigmentation Spotty hyperpigmentation Neoplasm of the gastrointestinal tract Agenesis of maxillary lateral incisor Facial telangiectasia in butterfly midface distribution Glaucoma IgG deficiency Telangiectasia of the skin Chronic leukemia Protruding ear Morbilliform rash Fluctuating hepatomegaly Fluctuating splenomegaly Normocytic hypoplastic anemia Pneumonia Polydactyly Prominent nose Pulmonary fibrosis Abnormality of the skin Hypertrichosis Abnormality of the face Bronchiectasis Sacral dimple High pitched voice Gynecomastia Neoplasm of the skin Visual impairment Scrotal hypoplasia Bradycardia Increased body weight Hypogonadotrophic hypogonadism Spontaneous abortion Narrow palpebral fissure Bicuspid aortic valve Nasal speech Psychosis Radial deviation of finger Emotional lability Inflammation of the large intestine Albinism Skeletal muscle hypertrophy Adrenal insufficiency Primary amenorrhea Decreased fetal movement Truncal obesity Small hand Stroke Carious teeth Delayed puberty Arachnodactyly Short palm Downturned corners of mouth Short foot Amenorrhea Tapered finger Sepsis Gastrointestinal hemorrhage Esotropia Febrile seizures Hip dysplasia Decreased muscle mass External genital hypoplasia Photophobia Temperature instability Poor fine motor coordination Anteverted ears Frontal upsweep of hair Erysipelas Disseminated intravascular coagulation Triangular mouth Central adrenal insufficiency Cor pulmonale Hypoplastic labia minora Psychotic episodes Narrow palm Hypopnea Poor gross motor coordination Acromicria Abdominal obesity Generalized hypopigmentation Polyphagia Iris hypopigmentation Narrow nasal bridge Impaired pain sensation Striae distensae Pulmonary embolism Hypopigmentation of hair Hypoventilation Abnormality of lipid metabolism Hypothermia Central hypotonia Overweight Oligomenorrhea Acrocyanosis Hypoplasia of the fovea Ocular albinism Abnormality of the pinna Micropenis Drooling Meningioma Lipoma Abnormality of the vasculature Papilledema Prolactin excess Skin tags Megalencephaly Hydrocele testis Renal cell carcinoma Furrowed tongue Astrocytoma Ovarian cyst Bone cyst Cellular immunodeficiency Long penis Hashimoto thyroiditis Thyroiditis Papilloma Intracranial hemorrhage Increased intracranial pressure Melanoma Breast carcinoma Goiter Incoordination Dysdiadochokinesis Cutis marmorata Ovarian neoplasm Macule Abnormality of the thyroid gland Multiple lipomas Cellulitis Hamartoma Hyperthyroidism Enlarged polycystic ovaries Fibroma Respiratory failure Conjunctival hamartoma Transitional cell carcinoma of the bladder Neoplasm of the thyroid gland Fibroadenoma of the breast Cutis marmorata telangiectatica congenita Enlarged cerebellum Dysplastic gangliocytoma of the cerebellum Ductal carcinoma in situ Mucosal telangiectasiae Merkel cell skin cancer Multiple trichilemmomata Lobular carcinoma in situ Hypertension Hyporeflexia Hyperactivity Acrokeratosis Pseudopapilledema Generalized hyperkeratosis Angioid streaks of the fundus Neoplasm of the central nervous system Decreased proportion of CD4-positive T cells Adenoma sebaceum Colonic diverticula Subcutaneous lipoma Abnormality of the penis Ovarian carcinoma Progressive macrocephaly Intestinal polyp Thyroid adenoma Varicocele Follicular thyroid carcinoma Endometrial carcinoma Colorectal polyposis Abnormality of the curvature of the vertebral column


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